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Merck

SAB1406114

Sigma-Aldrich

Anti-MDM4 antibody produced in mouse

purified immunoglobulin, buffered aqueous solution

Synonym(e):

DKFZp781B1423, HDMX, MDMX, MGC132766, MRP1

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About This Item

UNSPSC-Code:
12352203
NACRES:
NA.41

Biologische Quelle

mouse

Qualitätsniveau

Konjugat

unconjugated

Antikörperform

purified immunoglobulin

Antikörper-Produkttyp

primary antibodies

Klon

polyclonal

Form

buffered aqueous solution

Mol-Gew.

antigen ~54.9 kDa

Speziesreaktivität

human

Methode(n)

indirect immunofluorescence: suitable
western blot: 1 μg/mL

NCBI-Hinterlegungsnummer

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Lagertemp.

−20°C

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... MDM4(4194)

Verwandte Kategorien

Allgemeine Beschreibung

Mouse double minute 4 (MDM4), also known as MDMX, is encoded by the gene mapped to human chromosome 1q32.1. The encoded protein is a structural homolog of MDM2. It belongs to the MDM family.
The human MDM4 gene, which plays a role in apoptosis, encodes a 490-amino acid protein containing a RING finger domain and a putative nuclear localization signal. The MDM4 putative nuclear localization signal, which all Mdm proteins contain, is located in the C-terminal region of the protein. The mRNA is expressed at a high level in thymus and at lower levels in all other tissues tested. MDM4 protein produced by in vitro translation interacts with p53 via a binding domain located in the N-terminal region of the MDM4 protein. MDM4 shows significant structural similarity to p53-binding protein MDM2. Two transcript variants, one protein-coding and the other likely not to be protein-coding, have been found for this gene. (provided by RefSeq)

Immunogen

MDM4 (NP_002384.2, 1 a.a. ~ 490 a.a) full-length human protein.

Sequence
MTSFSTSAQCSTSDSACRISPGQINQVRPKLPLLKILHAAGAQGEMFTVKEVMHYLGQYIMVKQLYDQQEQHMVYCGGDLLGELLGRQSFSVKDPSPLYDMLRKNLVTLATATTDAAQTLALAQDHSMDIPSQDQLKQSAEESSTSRKRTTEDDIPTLPTSEHKCIHSREDEDLIENLAQDETSRLDLGFEEWDVAGLPWWFLGNLRSNYTPRSNGSTDLQTNQDVGTAIVSDTTDDLWFLNESVSEQLGVGIKVEAADTEQTSEEVGKVSDKKVIEVGKNDDLEDSKSLSDDTDVEVTSEDEWQCTECKKFNSPSKRYCFRCWALRKDWYSDCSKLTHSLSTSDITAIPEKENEGNDVPDCRRTISAPVVRPKDAYIKKENSKLFDPCNSVEFLDLAHSSESQETISSMGEQLDNLSEQRTDTENMEDCQNLLKPCSLCEKRPRDGNIIHGRTGHLVTCFHCARRLKKAGASCPICKKEIQLVIKVFIA

Biochem./physiol. Wirkung

Mouse double minute 4 (MDM4)/ MDMX acts as an essential regulator of the tumor suppressor Tp53. Overexpression of the gene has been observed in patients with hepatocellular carcinoma (HCC). Polymorphism in the gene increases the risk of susceptibility to gastric cancer (GCa). In addition, upregulated expression of the gene is also involved in the etiology of various cancers, such as invasive breast carcinoma liver hepatocellular carcinoma, retinoblastomas and skin cutaneous melanomas.

Physikalische Form

Solution in phosphate buffered saline, pH 7.4

Haftungsausschluss

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), 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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Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

MDM4 actively restrains cytoplasmic mTORC1 by sensing nutrient availability
Mancini F, et al.
Molecular Cancer, 16(1), 55-55 (2017)
Etiology?dependent molecular mechanisms in human hepatocarcinogenesis.
Schlaeger C, et al.
Hepatology, 47(2), 511-520 (2008)
MDM4 genetic variants and risk of gastric cancer in an eastern chinese population
Wang MY, et al.
Oncotarget, 8(12), 19547-19547 (2017)
The associations between MDM4 gene polymorphisms and cancer risk.
Wang MJ, et al.
Oncotarget, 7(34), 55611-55611 (2016)
A PRISMA-compliant meta-analysis of MDM4 genetic variants and cancer susceptibility
Zhai Y, et al.
Oncotarget, 7(45), 73935-73935 (2016)

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