TP53 (phospho S37) polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic phosphopeptide of TP53.
Immunogen
Synthetic phosphopeptide corresponding to residues surrounding S37 of human TP53.
Sequence
LPSPH
Host
Rabbit
Theoretical MW (kDa)
53
Reactivity
Human, Mouse, Rat
Specificity
This antibody recognizes ~53 KDa of human TP53 protein. It does not recognize non-phosphorylated peptides.
Form
Liquid
Quality Control Testing
Antibody Reactive Against Synthetic Peptide.
Recommend Usage
Western Blot (0.1-1 ug/mL)
ELISA (0.01-0.1 ug/mL)
Immunoprecipitation (2-5 ug/mL)
Immunohistochemistry (2-5 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In TBS, pH 7.2 (BSA, 10% Proclin300)
Storage Instruction
Store at 4°C. For long term storage store at -20°C or lower.
Aliquot to avoid repeated freezing and thawing. -
Applications
Western Blot (Cell lysate)
The cell lysate derived from UV stimulated HeLa cells was immunoprobed by TP53 (phospho S37) polyclonal antibody (Cat # PAB12641) at 1 : 500. An immunoreactive band is observed around ~ 53 KDa.Immunocytochemistry
Immunocytochemical staining of UV treated HeLa cells cultured in the cell chamber, fixed, and immunoprobed by TP53 (phospho S37) polyclonal antibody (Cat # PAB12641) at 1 : 100 for 10 min at RT.Immunoprecipitation
Enzyme-linked Immunoabsorbent Assay
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Gene Info — TP53
Entrez GeneID
7157Gene Name
TP53
Gene Alias
FLJ92943, LFS1, TRP53, p53
Gene Description
tumor protein p53
Gene Ontology
HyperlinkGene Summary
This gene encodes tumor protein p53, which responds to diverse cellular stresses to regulate target genes that induce cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. p53 protein is expressed at low level in normal cells and at a high level in a variety of transformed cell lines, where it's believed to contribute to transformation and malignancy. p53 is a DNA-binding protein containing transcription activation, DNA-binding, and oligomerization domains. It is postulated to bind to a p53-binding site and activate expression of downstream genes that inhibit growth and/or invasion, and thus function as a tumor suppressor. Mutants of p53 that frequently occur in a number of different human cancers fail to bind the consensus DNA binding site, and hence cause the loss of tumor suppressor activity. Alterations of this gene occur not only as somatic mutations in human malignancies, but also as germline mutations in some cancer-prone families with Li-Fraumeni syndrome. Multiple p53 variants due to alternative promoters and multiple alternative splicing have been found. These variants encode distinct isoforms, which can regulate p53 transcriptional activity. [provided by RefSeq
Other Designations
p53 antigen|p53 transformation suppressor|p53 tumor suppressor|phosphoprotein p53|transformation-related protein 53
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Interactome
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Pathway
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Disease
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Publication Reference
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Analysis of the anti-p53 antibody response in cancer patients.
Labrecque S, Naor N, Thomson D, Matlashewski G.
Cancer Research 1993 Aug; 53(15):3468.
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Analysis of the anti-p53 antibody response in cancer patients.
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