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Rabbit Recombinant Monoclonal PICK1 antibody. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra) and reacts with Mouse, Human samples.

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Images

Western blot - Anti-PICK1 antibody [EPR25155-48] (AB290727), expandable thumbnail
  • Western blot - Anti-PICK1 antibody [EPR25155-48] (AB290727), expandable thumbnail
  • Western blot - Anti-PICK1 antibody [EPR25155-48] (AB290727), expandable thumbnail
  • Immunoprecipitation - Anti-PICK1 antibody [EPR25155-48] (AB290727), expandable thumbnail
  • Immunocytochemistry/ Immunofluorescence - Anti-PICK1 antibody [EPR25155-48] (AB290727), expandable thumbnail

Key facts

Isotype
IgG
Host species
Rabbit
Storage buffer

pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA

Form
Liquid
Clonality
Monoclonal

Immunogen

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

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
ICC/IFIPWBIHC-PFlow Cyt (Intra)
Human
Not recommended
Tested
Tested
Not recommended
Not recommended
Mouse
Tested
Not recommended
Tested
Not recommended
Tested
Rat
Not recommended
Not recommended
Not recommended
Not recommended
Not recommended

Tested
Tested

Species
Mouse
Dilution info
1/50
Notes

-

Not recommended
Not recommended

Species
Human, Rat
Dilution info
-
Notes

-

Tested
Tested

Species
Human
Dilution info
1/30
Notes

-

Not recommended
Not recommended

Species
Mouse, Rat
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse
Dilution info
1/1000
Notes

-

Species
Human
Dilution info
1/1000
Notes

-

Not recommended
Not recommended

Species
Rat
Dilution info
-
Notes

-

Not recommended
Not recommended

Species
Mouse, Rat, Human
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse
Dilution info
1/500
Notes

-

Not recommended
Not recommended

Species
Human, Rat
Dilution info
-
Notes

-

Target data

Function

Probable adapter protein that bind to and organize the subcellular localization of a variety of membrane proteins containing some PDZ recognition sequence. Involved in the clustering of various receptors, possibly by acting at the receptor internalization level. Plays a role in synaptic plasticity by regulating the trafficking and internalization of AMPA receptors. May be regulated upon PRKCA activation. May regulate ASIC1/ASIC3 channel. Regulates actin polymerization by inhibiting the actin-nucleating activity of the Arp2/3 complex; the function is competitive with nucleation promoting factors and is linked to neuronal morphology regulation and AMPA receptor (AMPAR) endocytosis. Via interaction with the Arp2/3 complex involved in regulation of synaptic plasicity of excitatory synapses and required for spine shrinkage during long-term depression (LTD). Involved in regulation of astrocyte morphology, antagonistic to Arp2/3 complex activator WASL/N-WASP function.

Alternative names

PRKCABP, PICK1, PRKCA-binding protein, Protein interacting with C kinase 1, Protein kinase C-alpha-binding protein

Recommended products

Rabbit Recombinant Monoclonal PICK1 antibody. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra) and reacts with Mouse, Human samples.

Key facts

Isotype
IgG
Form
Liquid
Clonality
Monoclonal
Immunogen
  • The exact immunogen used to generate this antibody is proprietary information.
Clone number
EPR25155-48
Purification technique
Affinity purification Protein A
Concentration
Loading...

Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Notes

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

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.

Supplementary info

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

PICK1 or Protein Interacting with C Kinase 1 is a protein that plays a significant role in cellular processes. With a molecular mass of approximately 47 kDa PICK1 is well known for its ability to bind to proteins through its PDZ domain. You can find PICK1 expressed highly in the brain but it is also present in other tissues like the pancreas and testes. This makes it an important target for understanding various cellular interactions and functions related to protein trafficking.

Biological function summary

PICK1 is known for its role in modulating the trafficking and synaptic targeting of AMPA receptors which are essential for synaptic plasticity and memory formation. It operates as part of a protein complex that influences the receptor's presence at the synaptic membrane. PICK1 binds with proteins like GluA2 subunit of AMPA receptors which allows it to regulate receptor internalization and surface expression impacting synaptic signaling and plasticity.

Pathways

PICK1 interacts within the glutamatergic signaling and insulin secretion pathways. In the glutamatergic signaling pathway it contributes to the regulation of synaptic strength by linking with other proteins such as protein kinase C (PKC) to facilitate synapse dynamics. In insulin secretion PICK1 partners with proteins like the insulin granule docking machinery to regulate insulin release in response to glucose.

Associated diseases and disorders

Research has linked PICK1 function with conditions like schizophrenia and diabetes. PICK1's regulatory influence on AMPA receptors involves interactions with proteins such as protein kinase C which researchers have associated with synaptic abnormalities seen in schizophrenia. Regarding diabetes PICK1's role in insulin secretion connects it to the disease through the regulation of proteins involved in insulin granule dynamics. Understanding these connections aids in developing potential therapeutic strategies for these disorders.

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.

7 product images

  • Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727), expandable thumbnail

    Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    Blocking / Dilution buffer and concentration: 5% NFDM/TBST

    The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID 10027300；PMID: 32336285).

    All lanes: Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727) at 1/1000 dilution

    All lanes: HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg

    Secondary

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

    Predicted band size: 46 kDa

    Observed band size: 46 kDa

    Exposure time: 3min

  • Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727), expandable thumbnail

    Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    Blocking / Dilution buffer and concentration: 5% NFDM/TBST

    The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID 10027300；PMID: 32336285).

    All lanes: Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727) at 1/1000 dilution

    Lane 1: 293T (human embryonic kidney epithelial cell) transfected with scrambled siRNA control, whole cell lysate at 20 µg

    Lane 2: 293T transfected with siRNA specifically targeting PICK1, whole cell lysate at 20 µg

    Secondary

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

    Predicted band size: 46 kDa

    Observed band size: 46 kDa

    Exposure time: 3min

  • Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727), expandable thumbnail

    Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    Blocking / Diluent buffer and concentration: 5% NFDM/TBST

    The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID 10027300；PMID: 32336285).

    All lanes: Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727) at 1/1000 dilution

    Lane 1: C2C12 (mouse myoblasts myoblast) whole cell lysate at 20 µg

    Lane 2: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg

    Lane 3: RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg

    Secondary

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

    Predicted band size: 46 kDa

    Observed band size: 46 kDa

    Exposure time: 3min

  • Immunoprecipitation - Anti-PICK1 antibody [EPR25155-48] (ab290727), expandable thumbnail

    Immunoprecipitation - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    PICK1 was immunoprecipitated from 0.35 mg LNCaP (human prostate carcinoma epithelial cell) whole cell lysate 10 ug with ab290727 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab290727 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: LNCaP (human prostate carcinoma epithelial cell) whole cell lysate 10 ug

    Lane 2: ab290727 IP in LNCaP whole cell lysate

    Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of ab290727 in LNCaP whole cell lysate

    Blocking and dilution buffer and concentration: 5% NFDM/TBST.

    Exposure time: 3 minutes

    All lanes: Immunoprecipitation - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    Predicted band size: 46 kDa

  • Immunocytochemistry/ Immunofluorescence - Anti-PICK1 antibody [EPR25155-48] (ab290727), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeilized RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) cells lebelling PICK1 with ab290727 at 1/50 (10.2 ug/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 antibody at 1/1000 (2ug/mL) dilution (Green). Confocal image showing cytoplasmic staining in RAW 264.7 cell line is observed. Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5ug/ml) dilution (Red). The Nuclear counterstain was DAPI (Blue).

    Secondary antibody only control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2ug/mL) dilution.

  • Flow Cytometry (Intracellular) - Anti-PICK1 antibody [EPR25155-48] (ab290727), expandable thumbnail

    Flow Cytometry (Intracellular) - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cells labelling PICK1 with ab290727 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 1/2000 dilution was used as the secondary antibody.

  • Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727), expandable thumbnail

    Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727)

    PICK1 Western blot staining using rabbit Anti-PICK1 antibody

    Western blot: Rabbit Monoclonal[EPR25155-48] to PICK1 ab290727 staining at 1/1000 dilution, shown in green; Mouse anti GAPDH (Anti-GAPDH antibody [6C5] - Loading Control ab8245) loading control staining at 1/20,000 dilution, shown in magenta. A band was observed at 47 kDa in Wild-type U-87 MG cell lysates with no signal observed at this size in PICK1 knockout U-87 MG cell line. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 5pc Milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4°C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20,000 dilution.

    All lanes: Western blot - Anti-PICK1 antibody [EPR25155-48] (ab290727) at 1/1000 dilution

    Lane 1: Wild-type U-87 MG at 20 µg

    Lane 3: T-47D at 20 µg

    Lane 4: MCF7 at 20 µg

    Secondary

    All lanes: Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution

    Performed under reducing conditions.

    Predicted band size: 47 kDa

    Observed band size: 47 kDa

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Product protocols

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