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>   首页   >   产品   >   流式抗体   >   未偶联流式验证抗体   >   Recombinant Anti-IPP1 Rabbit mAb   

Recombinant Anti-IPP1 Rabbit mAb

     
  • 1 - Recombinant Anti-IPP1 Rabbit mAb AP94976
    Western blot analysis of IPP1 expression in Rat brain (A) whole cell lysates. (Predicted band size: 19 kD; Observed band size: 27 kD)
  • 3 - Recombinant Anti-IPP1 Rabbit mAb AP94976
    Immunofluorescent analysis of IPP1 staining in MCF7 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with an AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC, FC, IP, IF/IC
Primary Accession Q13522
Reactivity Human, Mouse, Rat
Host Rabbit
Clonality Monoclonal
Calculated MW 18939 Da
Additional Information
Gene ID 5502
Other Names IPP1; Protein phosphatase 1 regulatory subunit 1A; Protein phosphatase inhibitor 1; I-1; IPP-1
Target/Specificity KLH-conjugated synthetic peptide encompassing a sequence within human IPP1 protein. The exact sequence is proprietary.
Dilution WB~~WB (1/500 - 1/1000)
IHC~~1:100~500
FC~~1:10~50
IP~~N/A
IF/IC~~N/A
Format Liquid in PBS, pH 7.3, 50% glycerol, 0.05% BSA, and 0.05% Proclin300.
StorageStore at -20 °C.Stable for 12 months from date of receipt

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name PPP1R1A
Synonyms IPP1
Function Inhibitor of protein-phosphatase 1. This protein may be important in hormonal control of glycogen metabolism. Hormones that elevate intracellular cAMP increase I-1 activity in many tissues. I-1 activation may impose cAMP control over proteins that are not directly phosphorylated by PKA. Following a rise in intracellular calcium, I-1 is inactivated by calcineurin (or PP2B). Does not inhibit type-2 phosphatases.
Research Areas
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