Rabbit Recombinant Monoclonal PPR17 antibody. Carrier free. Suitable for IHC-P, WB, IP, IHC-Fr, mIHC and reacts with Mouse, Rat samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
IHC-P | WB | IP | Flow Cyt (Intra) | IHC-Fr | mIHC | |
---|---|---|---|---|---|---|
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 |
Species | Dilution info | Notes |
---|---|---|
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. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat, Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Inhibits phosphatase activities of protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A) complexes.
Gsbs, Protein phosphatase 1 regulatory subunit 17, G substrate
Rabbit Recombinant Monoclonal PPR17 antibody. Carrier free. Suitable for IHC-P, WB, IP, IHC-Fr, mIHC and reacts with Mouse, Rat samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
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:
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.
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.
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.
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.
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.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our 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.
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)
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)
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
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution
Exposure time: 180s
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)
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)
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
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
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
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
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
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
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
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
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
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
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
This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.
This data was developed using Anti-Ppp1r17 antibody [EPR29124-227] ab317831, the same antibody clone in a different buffer formulation.
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