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  • MDM2 Antibodies

OriGene

MDM2 Monoclonal Antibody (OTI1E6), TrueMAB™

View all (106) MDM2 antibodies

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Protocols
Questions & Answers

Cite MDM2 Monoclonal Antibody (OTI1E6), TrueMAB™

  • Antibody Testing Data (4)
MDM2 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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MDM2 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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MDM2 Antibody (TA801812) in IHC (P)

Immunohistochemical staining of paraffin-embedded human lymphoma tissue using anti-MDM2 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120°C for 3min, TA801812) {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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MDM2 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
MDM2 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
MDM2 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
MDM2 Antibody in Western Blot (WB)
MDM2 Monoclonal Antibody (OTI1E6), TrueMAB™

Product Details

TA801812

Applications
Tested Dilution
Publications

Western Blot (WB)

1:2,000
-

Immunohistochemistry (Paraffin) (IHC (P))

1:150
-
Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG1

Class

Monoclonal

Type

Antibody

Clone

OTI1E6

Immunogen

Human recombinant protein fragment corresponding to amino acids 119-438 of human MDM2 produced in E.coli.
View immunogen

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

Affinity chromatography

Storage buffer

PBS with 1% BSA, 50% glycerol

Contains

0.02% sodium azide

Storage conditions

-20°C, Avoid Freeze/Thaw Cycles

Shipping conditions

Ambient (domestic); Wet ice (international)

Target Information

MDM2 is a ubiquitin ligase for p53 and plays a central role in regulation of the stability of p53. MDM2 is located on chromosome 12 on the q arm. Akt-mediated phosphorylation of MDM2 at Ser166 and Ser186 increases its interaction with p300, allowing MDM2-mediated ubiquitination and degradation of p53. Phosphorylation of MDM2 also blocks its binding to p19ARF, increasing the degradation of p53. MDM2 has also been shown to negatively regulate p53 function. MDM2 binds and inhibits transactivation role played by p53 and overexpression of MDM2 can result in the inactivation of p53 and decrease its tumor suppressor function. Another process by which MDM2 can inactivate p53 is by degrading p53 as the protein also possesses E3 ubiquitin ligase activity. Further, MDM2 plays important roles in apoptosis and cell cycle. MDM2 is over expressed in a wide range of human malignancies including soft tissue carcinomas and breast cancer. In addition to p53, MDM2 is involved in processes of cell cycle, apoptosis, and tumorigenesis through interactions with proteins that include retinoblastoma 1 and ribosomal protein L5. More than 40 different alternatively spliced transcript variants of MDM2 have been isolated from both tumor and normal tissues.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: Double minute 2 protein; double minute 2, human homolog of; p53-binding protein; E3 ubiquitin-protein ligase Mdm2; Hdm2; HGNC:6973; human homolog of; MDM2 oncogene, E3 ubiquitin protein ligase; MDM2 proto-oncogene, E3 ubiquitin protein ligase; MDM2 variant FB28; Mdm2, p53 E3 ubiquitin protein ligase homolog; Mdm2, transformed 3T3 cell double minute 2, p53 binding protein; MGC5370; MGC71221; Oncoprotein Mdm2; OTTHUMP00000183490; OTTHUMP00000183492; OTTHUMP00000183494; OTTHUMP00000183495; OTTHUMP00000183496; OTTHUMP00000183497; p53-binding protein Mdm2; RING-type E3 ubiquitin transferase Mdm2

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Gene Aliases: ACTFS; hdm2; HDMX; MDM2

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UniProt ID: (Human) Q00987

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Entrez Gene ID: (Human) 4193

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Function(s)
p53 binding ubiquitin-protein transferase activity protein binding zinc ion binding ligase activity SUMO transferase activity enzyme binding ubiquitin protein ligase binding identical protein binding peroxisome proliferator activated receptor binding ubiquitin protein ligase activity scaffold protein binding
Process(es)
negative regulation of transcription from RNA polymerase II promoter blood vessel development blood vessel remodeling regulation of heart rate atrioventricular valve morphogenesis endocardial cushion morphogenesis ventricular septum development atrial septum development protein complex assembly DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest traversing start control point of mitotic cell cycle positive regulation of cell proliferation response to toxic substance response to carbohydrate response to iron ion positive regulation of gene expression negative regulation of protein processing viral process protein ubiquitination protein sumoylation peptidyl-lysine modification protein destabilization response to magnesium ion positive regulation of proteasomal ubiquitin-dependent protein catabolic process protein localization to nucleus regulation of protein catabolic process response to cocaine response to drug protein ubiquitination involved in ubiquitin-dependent protein catabolic process negative regulation of cysteine-type endopeptidase activity involved in apoptotic process response to morphine negative regulation of DNA damage response, signal transduction by p53 class mediator establishment of protein localization response to ether negative regulation of transcription, DNA-templated positive regulation of mitotic cell cycle response to antibiotic positive regulation of protein export from nucleus response to steroid hormone cardiac septum morphogenesis cellular response to hydrogen peroxide negative regulation of cell cycle arrest cellular response to antibiotic cellular response to vitamin B1 cellular response to alkaloid cellular response to growth factor stimulus cellular response to peptide hormone stimulus cellular response to estrogen stimulus cellular response to hypoxia cellular response to UV-C regulation of signal transduction by p53 class mediator negative regulation of signal transduction by p53 class mediator
It has to be done as per old AB suggested Products section.
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