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Key Documents

M4308

Sigma-Aldrich

Monoclonal Anti-MDM2 antibody produced in mouse

clone SMP14, ascites fluid

Synonyme(s) :

Anti-ACTFS, Anti-HDMX, Anti-LSKB, Anti-hdm2

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

mouse

Niveau de qualité

Conjugué

unconjugated

Forme d'anticorps

ascites fluid

Type de produit anticorps

primary antibodies

Clone

SMP14, monoclonal

Poids mol.

antigen ~90 kDa (additional band of approx. 55 kDa)

Contient

15 mM sodium azide

Espèces réactives

human, rat, mouse (weak)

Technique(s)

immunocytochemistry: suitable
immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
immunohistochemistry (frozen sections): suitable
immunoprecipitation (IP): suitable
indirect ELISA: suitable
microarray: suitable
western blot: 1:1,000 using a whole extract of transfected 293T (human embryonal kidney) cells expressing human MDM2

Isotype

IgG1

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... MDM2(4193)
mouse ... Mdm2(17246)
rat ... Mdm2(246362)

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Description générale

Monoclonal Anti-MDM2 (mouse IgG1 isotype) is derived from the SMP14 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from a BALB/c mouse. The murine double minute (mdm2), an E3 ubiquitin ligase comprises an N-terminal p53 domain. The C-terminal domain encompasses the really interesting new gene (RING) domain, nuclear localization signal (NLS), nucleolar localization signal (NoLS) and a nuclear export signal (NES). MDM2 is mapped to the human chromosome 12q15. It is expressed as different splice variants.

Spécificité

Detects the MDM2 protein alone or in complex with E2F1, p53, and retinoblastoma proteins. A slight cross-reactivity is observed with cytokeratins 6, 14, and 16.

Immunogène

synthetic peptide corresponding to amino acids 154-167 of human MDM2 conjugated to KLH.

Application

Monoclonal Anti-MDM2 antibody produced in mouse has been used in:
  • immunoblotting
  • immunoprecipitation (1 μg/ml)
  • fluorescence-activated cell sorting (FACS)
  • immunofluorescence (1:200)
  • immunohistochemistry
  • confocal immunofluorescence
  • immunocytochemistry
  • enzyme-linked immunosorbent assay (ELISA)

Actions biochimiques/physiologiques

Murine double minute (mdm2) mediates the transactivation of the tumor suppressor p53. MDM2 binds to the histone acetyltransferase p300 transcriptional coactivator/histone acetylase to mediate the degradation of p53. The nuclear localization signal of MDM2 mediates its shuttling from the nucleus to the cytoplasm and mediates p53 degradation. In addition to its relationships with p53, MDM2 activates cell proliferation by stimulating the S-phase-inducing transcription factors, E2F1/dimerization partner 1 (DP1). The amplification of the MDM2 gene is detected in the esophagogastric, liver, colon, breast and lung carcinomas. A disturbance in the optimal levels of the MDM2/p53 axis may have an impact on premature aging. Monoclonal antibody reacting specifically with MDM2 is an essential tool in defining the interactions and distributions of MDM2, its function in signaling pathways and mutual regulation of p53.

Forme physique

Monoclonal Anti-MDM2 is supplied as ascites fluid containing 15 mM sodium azide.

Stockage et stabilité

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. Storage in "frost-free" freezers 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.

Clause de non-responsabilité

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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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Les clients ont également consulté

Jiabing Li et al.
Cell death & disease, 14(11), 783-783 (2023-11-30)
Li-Fraumeni syndrome (LFS) is characterized by germline mutations occurring on one allele of genome guardian TP53. It is a severe cancer predisposition syndrome with a poor prognosis, partly due to the frequent development of subsequent primary tumors following DNA-damaging therapies.
Rasoul Pourebrahim et al.
Cell reports. Medicine, 5(5), 101558-101558 (2024-05-12)
The investigation of the mechanisms behind p53 mutations in acute myeloid leukemia (AML) has been limited by the lack of suitable mouse models, which historically have resulted in lymphoma rather than leukemia. This study introduces two new AML mouse models.
Atsunori Oga et al.
Oncology reports, 26(6), 1393-1398 (2011-09-07)
We analyzed 10 adenoid cystic carcinomas (ACCs) of the salivary glands by array-based comparative genomic hybridization (a-CGH) using DNA chips spotted
Y Zhou et al.
Oncogene, 37(8), 1086-1094 (2017-11-07)
Esophageal squamous cell carcinoma (ESCC) is highly prevailing in Asia and it is ranked in the most aggressive squamous cell carcinomas. High-frequency loss of heterozygosity occurred in chromosome 14q11.2 in many tumors including ESCC, suggesting that one or more tumor-suppressor
Jiajia Zhou et al.
Nature immunology, 22(4), 460-470 (2021-03-27)
Targeting the p53-MDM2 pathway to reactivate tumor p53 is a chemotherapeutic approach. However, the involvement of this pathway in CD8+ T cell-mediated antitumor immunity is unknown. Here, we report that mice with MDM2 deficiency in T cells exhibit accelerated tumor

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