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Merck
CN

SAB4200852

Anti-p53 antibody, Mouse monoclonal

clone BP53-12, purified from hybridoma cell culture

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About This Item

NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
BP53-12, monoclonal
Application:
IF
Citations:
3
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Quality Level

conjugate

unconjugated

antibody form

purified from hybridoma cell culture

antibody product type

primary antibodies

clone

BP53-12, monoclonal

species reactivity

human

concentration

~1 mg/mL

technique(s)

immunoblotting: 0.06-0.125 μg/mL using human epidermoid carcinoma A431 cell line whole extract, immunofluorescence: 0.25-0.5 μg/mL using human A431cells

isotype

IgG2a

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... TP53(7157)

General description

The p53 protein was first identified in a complex with the simian virus 40 (SV40) large T-antigen.4-5 p53 is classified as a key tumor suppressor and is the most commonly mutated gene in human cancers; it is mutated in over 50% of all human cancers.6 Due to its central role in the DNA damage response (DDR), p53 is often referred to as the “guardian of the genome” and is suggested to be the most studied human gene of all time.7-8 p53 mutations are frequent in breast, lung, colon, ovarian, brain, testicular and bladder cancers, melanoma, neurofibrosarcoma and certain types of leukemia1-8.

Application

The antibody may be used in various immunochemical techniques including Immunoblotting (~53 kDa), Immunofluorescence, Immunoprecipitation1, Immunohistochemistry2 and ChIP3.

Biochem/physiol Actions

Monoclonal Anti-p53 antibody specifically recognizes a denaturation-resistant epitope on the primate p53 nuclear protein and does not react with other cellular proteins."
The human wild-type p53 protein is a 393 amino acid nuclear phosphoprotein present in the nucleus of all normal mammalian cells where it appears to be involved in the regulation of cell proliferation. The normal protein has a very short half-life and is present in only minute amounts in normal tissues and cells. In contrast, mutant p53 protein produced by malignant cells is usually a product of a point mutation in the p53 gene leading to substitution of a single amino acid that significantly prolongs the half-life of the protein. The accumulation of high levels of p53 is a potential novelmarker for malignancy.

Physical form

Supplied as a solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide as a preservative.Antibody Concentration: ∼ 1.0 mg/mL

Preparation Note

For continuous use, store at 2-8°C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

Disclaimer

Unless otherwise stated in our catalog  our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.


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Storage Class

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

低风险生物材料
常规特殊物品

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The most popular genes in the human genome.
Elie Dolgin
Nature, 551(7681), 427-431 (2017-11-24)
J Bártek et al.
Oncogene, 6(9), 1699-1703 (1991-09-01)
Accumulation of the p53 protein was analysed in 212 human malignant lesions. Immunohistochemical staining with new polyclonal (CM-1) and monoclonal antibodies (BP 53-12 and BP53-24) to p53 on methacarn-fixed paraffin sections showed positive staining in 161 (76%). The positive tumours
Meng Wu et al.
Oncology letters, 15(4), 5175-5180 (2018-03-20)
TAp73 and p53 are involved in regulating tumor angiogenesis and vasohibin-1 (VASH1) is an anti-angiogenic factor. Whether TAp73 regulates angiogenesis positively or negatively is controversial. The status of P53 may determine the effect of TAp73 on angiogenesis. To the best