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Rabbit Recombinant Monoclonal PPR17 antibody. Carrier free. Suitable for IHC-P, WB, IP, IHC-Fr, mIHC and reacts with Mouse, Rat samples.

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Images

Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (AB317832), expandable thumbnail
  • Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (AB317832), expandable thumbnail
  • Immunoprecipitation - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (AB317832), expandable thumbnail
  • Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (AB317832), expandable thumbnail
  • Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (AB317832), expandable thumbnail

Key facts

Isotype
IgG
Host species
Rabbit
Storage buffer

pH: 7.2 - 7.4
Constituents: 100% PBS

Form
Liquid
Clonality
Monoclonal

Immunogen

  • The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
IHC-PWBIPFlow Cyt (Intra)IHC-FrmIHC
Human
Not recommended
Not recommended
Not recommended
Not recommended
Not recommended
Not recommended
Mouse
Tested
Tested
Tested
Not recommended
Tested
Tested
Rat
Tested
Tested
Expected
Not recommended
Tested
Tested

Tested
Tested

Species
Mouse
Dilution info
-
Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Species
Rat
Dilution info
-
Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Not recommended
Not recommended

Species
Human
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse, Rat
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Human
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse
Dilution info
-
Notes

-

Expected
Expected

Species
Rat
Dilution info
Use at an assay dependent concentration.
Notes

-

Not recommended
Not recommended

Species
Human
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Mouse, Rat, Human
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse, Rat
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Human
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse, Rat
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Human
Dilution info
-
Notes

-

Target data

Function

Inhibits phosphatase activities of protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A) complexes.

Alternative names

Recommended products

Rabbit Recombinant Monoclonal PPR17 antibody. Carrier free. Suitable for IHC-P, WB, IP, IHC-Fr, mIHC and reacts with Mouse, Rat samples.

Key facts

Isotype
IgG
Form
Liquid
Clonality
Monoclonal
Immunogen
  • The exact immunogen used to generate this antibody is proprietary information.
Carrier free
Yes
Clone number
EPR29124-227
Purification technique
Affinity purification Protein A
Concentration
Loading...

Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Notes

ab317832 is the carrier-free version of Anti-Ppp1r17 antibody [EPR29124-227] ab317831.

Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.

Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.

Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.
Activity summary

Ppp1r17 also known as Protein Phosphatase 1 Regulatory Subunit 17 is a regulatory protein that modifies the activity of protein phosphatase 1 (PP1). It weighs approximately 10.5 kDa. Ppp1r17 acts by inhibiting PP1's ability to dephosphorylate its substrate proteins. It is expressed predominantly in the cerebellum and to some extent in other brain areas. The ability of Ppp1r17 to regulate PP1 suggests its importance in finely tuning brain functions and activities.

Biological function summary

Ppp1r17 serves a regulatory function in neuronal signaling and synaptic plasticity. It is not known to be part of a larger protein complex but rather it exists as a regulatory component modulating PP1 activity. Ppp1r17 plays a role in the regulation of signal transduction impacting processes such as synaptic strength and plasticity which are key for learning and memory in the brain. Its expression pattern reflects its potential involvement in modulating neuronal function and possibly other cell signaling processes.

Pathways

Ppp1r17 participates primarily in neuronal signaling cascades. It is involved in pathways linked to the modulation of synaptic plasticity and learning processes such as long-term potentiation and depression. Through these pathways Ppp1r17 is associated with proteins like PP1 itself and those involved in the regulation of synaptic strength such as NMDA receptors. This places Ppp1r17 within significant neuronal signaling frameworks that dictate responses to stimuli and environmental learning.

Associated diseases and disorders

Ppp1r17's regulation of PP1 activity links it to neurological conditions like cerebellar ataxia and potentially schizophrenia. Misregulation of PP1 activity often affected by modifications in Ppp1r17 function can result in altered neuronal activity and contribute to these disorders. The interaction between Ppp1r17 and PP1 can be further connected to proteins like DARPP-32 which also influence dopaminergic neurotransmission and are implicated in neuropsychiatric conditions. By affecting these essential pathways and processes Ppp1r17's functional integrity is critical for maintaining healthy brain physiology.

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

Full details and terms and conditions can be found here:
Terms & Conditions.

16 product images

  • Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    Ppp1r17 Immunohistochemistry (Frozen sections) staining of Mouse cerebellum (perfused-fixed) using rabbit Anti-Ppp1r17 antibody

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized Mouse cerebellum (perfused-fixed) tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at a 1/500 (1.046 µg/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at a 1/1000 (2 µg/mL) dilution.

    Panel A: merged staining of anti-Ppp1r17 (Anti-Ppp1r17 antibody [EPR29124-227] ab317831, green), anti-NeuN (Alexa Fluor® 647 Anti-NeuN antibody [EPR12763] - Neuronal Marker ab190565, grey) and anti-GFAP (Alexa Fluor® 594 Anti-GFAP antibody [EPR1034Y] - Astrocyte Marker ab201732, magenta) on mouse cerebellum.
    Panel B: anti-Ppp1r17 stained on mouse cerebellum.
    Panel C: anti-NeuN stained in neurons of mouse cerebellum.
    Panel D: anti-GFAP stained in astrocytes of mouse cerebellum.

    The section was incubated in two rounds of staining: in the order of Anti-Ppp1r17 antibody [EPR29124-227] ab317831 and Alexa Fluor® 647 Anti-NeuN antibody [EPR12763] - Neuronal Marker ab190565, Alexa Fluor® 594 Anti-GFAP antibody [EPR1034Y] - Astrocyte Marker ab201732 for 1 hr at room temperature. The nuclear counterstain was DAPI (Blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

    Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20)

  • Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    Ppp1r17 Immunohistochemistry (Frozen sections) staining of Rat cerebellum (perfused-fixed) using rabbit Anti-Ppp1r17 antibody

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized Rat cerebellum (perfused-fixed) tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at a 1/500 (1.046 µg/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at a 1/1000 (2 µg/mL) dilution.

    Panel A: merged staining of anti-Ppp1r17 (Anti-Ppp1r17 antibody [EPR29124-227] ab317831, green), anti-NeuN (Alexa Fluor® 647 Anti-NeuN antibody [EPR12763] - Neuronal Marker ab190565, grey) and anti-GFAP (Alexa Fluor® 594 Anti-GFAP antibody [EPR1034Y] - Astrocyte Marker ab201732, magenta) on rat cerebellum.
    Panel B: anti-Ppp1r17 stained on rat cerebellum.
    Panel C: anti-NeuN stained in neurons of rat cerebellum.
    Panel D: anti-GFAP stained in astrocytes of rat cerebellum.

    The section was incubated in two rounds of staining: in the order of Anti-Ppp1r17 antibody [EPR29124-227] ab317831 and Alexa Fluor® 647 Anti-NeuN antibody [EPR12763] - Neuronal Marker ab190565, Alexa Fluor® 594 Anti-GFAP antibody [EPR1034Y] - Astrocyte Marker ab201732 for 1 hr at room temperature. The nuclear counterstain was DAPI (Blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

    Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20)

  • Immunoprecipitation - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunoprecipitation - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Ppp1r17 was immunoprecipitated from 0.35 mg Mouse cerebellum tissue lysate with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.

    Lane 1: Mouse cerebellum tissue lysate

    Lane 2: Anti-Ppp1r17 antibody [EPR29124-227] ab317831 IP in Mouse cerebellum tissue lysate

    Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-Ppp1r17 antibody [EPR29124-227] ab317831 in Mouse cerebellum tissue lysate

    All lanes: Immunoprecipitation - Anti-Ppp1r17 antibody [EPR29124-227] (Anti-Ppp1r17 antibody [EPR29124-227] ab317831) at 1/30 dilution

    All lanes: Mouse cerebellum tissue lysate

    Secondary

    All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution

    Exposure time: 180s

  • Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized Rat liver (perfused-fixed) tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at a 1/500 (1.046 µg/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at a 1/1000 (2 µg/mL) dilution.

    Negative control: confocal image showing no staining on rat liver. The nuclear counterstain was DAPI (Blue). The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

    Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20)

  • Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Frozen sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized Mouse liver (perfused-fixed) tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at a 1/500 (1.046 µg/ml) dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at a 1/1000 (2 µg/mL) dilution.

    Negative control: confocal image showing no staining on mouse liver. The nuclear counterstain was DAPI (Blue). The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

    Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20)

  • Western blot - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Western blot - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Negative control: cerebral cortex, liver, lung.

    In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.

    All lanes: Western blot - Anti-Ppp1r17 antibody [EPR29124-227] (Anti-Ppp1r17 antibody [EPR29124-227] ab317831) at 1/1000 dilution

    Lane 1: Mouse brain tissue lysate at 20 µg with NFDM/TBST

    Lane 2: Mouse cerebellum tissue lysate at 20 µg with NFDM/TBST

    Lane 3: Mouse cerebral cortex tissue lysate at 20 µg with NFDM/TBST

    Lane 4: Mouse liver tissue lysate at 20 µg with NFDM/TBST

    Lane 5: Mouse lung tissue lysate at 20 µg with NFDM/TBST

    Secondary

    All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

    Developed using the ECL technique.

    Observed band size: 23 kDa, 36 kDa

    Exposure time: 92s

  • Western blot - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Western blot - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Negative control: cerebral cortex, liver, spleen.

    In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.

    All lanes: Western blot - Anti-Ppp1r17 antibody [EPR29124-227] (Anti-Ppp1r17 antibody [EPR29124-227] ab317831) at 1/1000 dilution

    Lane 1: Rat cerebellum tissue lysate at 20 µg with NFDM/TBST

    Lane 2: Rat cerebral cortex tissue lysate at 20 µg with NFDM/TBST

    Lane 3: Rat liver tissue lysate at 20 µg with NFDM/TBST

    Lane 4: Rat spleen tissue lysate at 20 µg with NFDM/TBST

    Secondary

    All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

    Developed using the ECL technique.

    Observed band size: 23 kDa, 36 kDa

    Exposure time: 180s

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of paraffin-embedded Mouse cerebellum tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 (0.262 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Positive staining on mouse cerebellum (PMID: 9920894, 22340725).

    The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 30 mins at room temperature.

    The immunostaining was performed on a Leica Biosystems BOND® RX instrument

    Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background

    Counterstained with Hematoxylin.

    Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of paraffin-embedded Mouse hypothalamus tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 (0.262 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Positive staining on mouse hypothalamus (PMID: 9920894, 22340725, 33753517).

    The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 30 mins at room temperature.

    The immunostaining was performed on a Leica Biosystems BOND® RX instrument

    Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background

    Counterstained with Hematoxylin.

    Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of paraffin-embedded Mouse whole brain (sagittal plane) tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 (0.262 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Positive staining on cerebellum and hypothalamus of mouse whole brain section (PMID: 9920894, 22340725, 33753517).

    The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 30 mins at room temperature.

    The immunostaining was performed on a Leica Biosystems BOND® RX instrument

    Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background

    Counterstained with Hematoxylin.

    Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of paraffin-embedded Rat cerebellum tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 (0.262 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Positive staining on rat cerebellum.

    The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 30 mins at room temperature.

    The immunostaining was performed on a Leica Biosystems BOND® RX instrument

    Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background

    Counterstained with Hematoxylin.

    Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of paraffin-embedded Rat hypothalamus tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 (0.262 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Positive staining on rat hypothalamus.

    The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 30 mins at room temperature.

    The immunostaining was performed on a Leica Biosystems BOND® RX instrument

    Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background

    Counterstained with Hematoxylin.

    Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 (0.262 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Negative control: no staining on mouse liver.

    The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 30 mins at room temperature.

    The immunostaining was performed on a Leica Biosystems BOND® RX instrument

    Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background

    Counterstained with Hematoxylin.

    Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.

    Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling Ppp1r17 with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 (0.262 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Negative control: no staining on rat liver.

    The section was incubated with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 for 30 mins at room temperature.

    The immunostaining was performed on a Leica Biosystems BOND® RX instrument

    Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background

    Counterstained with Hematoxylin.

    Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).

    Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins

  • Multiplex immunohistochemistry - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Multiplex immunohistochemistry - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.


    Multiplex immunohistochemistry analysis of Formalin/PFA-fixed paraffin-embedded sections of Mouse cerebellum tissue staining with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 dilution, Anti-KCNA antibody [EPR26383-85] ab313624 at 1/4000 dilution, Anti-Kv4.2/KCND2 antibody [EPR26384-89] ab307710 at 1/2000 dilution. Secondary used was Opal Polymer HRP Ms + Rb.
    Panel A: merged staining of anti-Ppp1r17 (magenta; Opal™690), anti-KCNA2 (green; Opal™520) and anti-KCND2 (gray; Opal™570) on mouse cerebellum.
    Panel B: anti-Ppp1r17 staining the Purkinje cells in mouse cerebellum.
    Panel C: anti-KCNA2 staining the basket cells in mouse cerebellum.
    Panel D: anti-KCND2 staining the granule cell layer in mouse cerebellum.
    Nuclear DNA was labeled with DAPI (shown in blue).
    The section was incubated in three rounds of staining: in the order of Anti-Ppp1r17 antibody [EPR29124-227] ab317831, Anti-KCNA antibody [EPR26383-85] ab313624 and Anti-Kv4.2/KCND2 antibody [EPR26384-89] ab307710 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
    The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
  • Multiplex immunohistochemistry - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832), expandable thumbnail

    Multiplex immunohistochemistry - Anti-Ppp1r17 antibody [EPR29124-227] - BSA and Azide free (ab317832)

    This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.


    Multiplex immunohistochemistry analysis of Formalin/PFA-fixed paraffin-embedded sections of Rat cerebellum tissue staining with Anti-Ppp1r17 antibody [EPR29124-227] ab317831 at 1/2000 dilution, Anti-KCNA antibody [EPR26383-85] ab313624 at 1/4000 dilution, Anti-Kv4.2/KCND2 antibody [EPR26384-89] ab307710 at 1/2000 dilution. Secondary used was Opal Polymer HRP Ms + Rb.
    Panel A: merged staining of anti-Ppp1r17 (magenta; Opal™690), anti-KCNA2 (green; Opal™520) and anti-KCND2 (gray; Opal™570) on rat cerebellum.
    Panel B: anti-Ppp1r17 staining the Purkinje cells in rat cerebellum.
    Panel C: anti-KCNA2 staining the basket cells in rat cerebellum.
    Panel D: anti-KCND2 staining the granule cell layer in rat cerebellum.
    Nuclear DNA was labeled with DAPI (shown in blue).
    The section was incubated in three rounds of staining: in the order of Anti-Ppp1r17 antibody [EPR29124-227] ab317831, Anti-KCNA antibody [EPR26383-85] ab313624 and Anti-Kv4.2/KCND2 antibody [EPR26384-89] ab307710 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
    The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.

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