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PHOSPHO-SMAD2 (S465, S467) PAB 100 UL BIOSOURCE (TM)

 
包装:
运保温度: -20°C
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描述:

Details
Tested species reactivity Human , Mouse
Published species reactivity Human , Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen The antiserum was produced against a chemically synthesized phosphopeptide derived from a region of human Smad2 that contains serines 465 and 467. The sequence is conserved in mouse and rat.
Conjugate Unconjugated
Form Liquid
Purification Antigen affinity chromatography
Storage buffer Dulbecco's PBS, pH 7.3, with 1mg/ml BSA, 50% glycerol
Contains 0.05% sodium azide
Storage Conditions -20°C
Tested Applications Dilution *
ChIP assay (ChIP) 10µl
Flow Cytometry (Flow) 3-5 µg/million cells
Immunocytochemistry (ICC) 1µg/mL
Immunofluorescence (IF) 1µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:20-1:200
Western Blot (WB) 1:500-1:2000

* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.

Published Applications  
Western Blot (WB) See 2 publications below

Background/Target Information

SMAD2, also known as MADH2 or MAD2 regulates multiple cellular processes, such as cell proliferation, apoptosis, and differentiation. Smad2 interacts with the TGF-beta receptors through its interaction with the SMAD anchor for receptor activation into the nucleus is a central event in TGF beta signaling. Phosphorylation of threonine 8 in the calmodulin-binding region of the MH1 domain by extracellular signalregulated kinase 1 (ERK1) enhances Smad2 transcriptional activity, which is negatively regulated by calmodulin.

 


注意事项:

For Research Use Only. Not for use in diagnostic procedures. 
 


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