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N6539

Sigma-Aldrich

Anti-NUMB (C-terminal) antibody produced in rabbit

~1.0 mg/mL, affinity isolated antibody

Sinônimo(s):

Anti-S171

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

fonte biológica

rabbit

Nível de qualidade

conjugado

unconjugated

forma do anticorpo

affinity isolated antibody

tipo de produto de anticorpo

primary antibodies

clone

polyclonal

peso molecular

antigen ~70 kDa

reatividade de espécies

human, rat

embalagem

antibody small pack of 25 μL

concentração

~1.0 mg/mL

técnica(s)

western blot: 1-2 μg/mL using rat brain extract (S1 fraction) and A431 cell lysate

nº de adesão UniProt

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

modificação pós-traducional do alvo

unmodified

Informações sobre genes

human ... NUMB(8650)
mouse ... Numb(18222)
rat ... Numb(29419)

Descrição geral

Numb gene with 13 exons is mapped to human chromosome 14q24.3. The protein comprises 651 amino acids. It belongs to the clathrin-associated sorting protein family with two domains namely phosphotyrosine-binding (PTB) and proline-rich region (PRR) domain. Mammalian Numb gene gives rise to at least four alternatively spliced transcripts that produce four protein isoforms Numb1-4, ranging from 65 to 72 kDa.
Numb homolog-NUMB is an adaptor protein and is aberrantly expressed in cancers.

Aplicação

Anti-NUMB (C-terminal) antibody produced in rabbit has been used in immunoblotting.

Ações bioquímicas/fisiológicas

Numb homolog-NUMB may act as a tumor suppressor. It also takes part in determining the cell fate. NUMB is involved in the endocytosis and trafficking of receptors.
Numb is a critical Notch antagonist and a conserved adapter protein that plays a role in the self-renewal of NSCs and neural differentiation in the central nervous system (CNS). In neural progenitors of CNS, the functional loss of numb is implicated in embryonic lethality accompanied by precocious neuronal differentiation. It has been suggested that a switch in numb isoform expression is a critical step in cortical development. Numb1 or numb3 isoforms that contain an insertion in the proline-rich region (PRRL), promote the proliferation of neural crest stem cells (NCSCs). Numb2 or numb4 isoforms without PRR insertions (PRRS) show ectopic expression and promote neuronal differentiation.

forma física

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Exoneração de responsabilidade

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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Código de classe de armazenamento

10 - Combustible liquids

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Visite a Biblioteca de Documentos

Jin Sima et al.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 36(4), 2885-2892 (2014-12-07)
The objective of the study was to investigate the impact of Numb on cell growth, cell migration, and invasion in human clear cell renal cell carcinoma (ccRCC). Endogenous expression of Numb was evaluated in the ccRCC cell lines (786-O, Caki-1
The association of cholesterol absorption gene numb polymorphism with coronary artery disease among Han Chinese and Uighur Chinese in Xinjiang, China
Abudoukelimu M, et al.
Lipids in Health and Disease, 14(1), 120-120 (2015)
Jonathan R Krieger et al.
Proteomics, 15(2-3), 434-446 (2014-11-19)
Numb is an adaptor protein that functions in the endocytosis and intracellular trafficking of membrane receptors and adhesion molecules. Previous studies have indicated that Numb localization and function are regulated through phosphorylation by atypical protein kinase C at several key
Notch: from neural development to neurological disorders
Lathia JD, et al.
Journal of Neurochemistry, 107(6), 1471-1481 (2008)
Phenotypic and genetic characterization of a patient with a de novo interstitial 14q24. 1q24. 3 deletion
Tassano E, et al.
Molecular Cytogenetics, 7(1), 49-49 (2014)

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