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Recombinant Rabbit Anti-ATR (p-S428) Monoclonal Antibody
Recombinant Rabbit Anti-ATR (p-S428) Monoclonal Antibody
ATR_HUMAN; ATR; Ataxia telangiectasia and Rad3-related protein; FRAP-related protein 1; 2.7.11.1; FRP1; ATR_MOUSE; Kiaa4069; ATR checkpoint kinase; ataxia telangiectasia and Rad3 related; MEC1, mitosis entry checkpoint 1, homolog (S. cerevisiae); Serine/t
Total $200.0
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  • NO.:SLA3402M
    React Species:Human, Mouse, Rat
    Immunogen Species:Rabbit
    Clonality:Recombinant
    Applications:WB, IHC-P, IHC-F, IF, ELISA
    Gene name:ATR (p-S428)
    UniProt Entry:Q13535
    NCBI Gene Entry:545
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Product NameRecombinant Rabbit Anti-ATR (p-S428) Monoclonal Antibody
Cat No.SLA3402M
AliasATR_HUMAN; ATR; Ataxia telangiectasia and Rad3-related protein; FRAP-related protein 1; 2.7.11.1; FRP1; ATR_MOUSE; Kiaa4069; ATR checkpoint kinase; ataxia telangiectasia and Rad3 related; MEC1, mitosis entry checkpoint 1, homolog (S. cerevisiae); Serine/threonine-protein kinase ATR
Host SpeciesRabbit
IsotypeIgG
ClonalityMonoclonal
Clone No.8H8
React SpeciesHuman,Mouse,Rat
ApplicationsWB (1:500-2000)
IHC-P (1:50-200)
IHC-F (1:50-200)
IF (1:50-200)
ELISA (1:5000-10000)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
Purificationaffinity purified by Protein A
Gene ID545
Swiss-ProtQ13535
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
BackgroundThe protein encoded by this gene belongs the PI3/PI4-kinase family, and is most closely related to ATM, a protein kinase encoded by the gene mutated in ataxia telangiectasia. This protein and ATM share similarity with Schizosaccharomyces pombe rad3, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. This kinase has been shown to phosphorylate checkpoint kinase CHK1, checkpoint proteins RAD17, and RAD9, as well as tumor suppressor protein BRCA1. Mutations of this gene are associated with Seckel syndrome. An alternatively spliced transcript variant of this gene has been reported, however, its full length nature is not known. Transcript variants utilizing alternative polyA sites exist. [provided by RefSeq, Jul 2008],
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

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