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安全性情報

N6539

Sigma-Aldrich

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

~1.0 mg/mL, affinity isolated antibody

別名:

抗S171抗体

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About This Item

UNSPSCコード:
12352203
NACRES:
NA.41

由来生物

rabbit

品質水準

結合体

unconjugated

抗体製品の状態

affinity isolated antibody

抗体製品タイプ

primary antibodies

クローン

polyclonal

分子量

antigen ~70 kDa

交差性

human, rat

包装

antibody small pack of 25 μL

濃度

~1.0 mg/mL

テクニック

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

UniProtアクセッション番号

輸送温度

dry ice

保管温度

−20°C

ターゲットの翻訳後修飾

unmodified

遺伝子情報

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

詳細

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.

アプリケーション

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

生物化学的/生理学的作用

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.

物理的形状

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

免責事項

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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保管分類コード

10 - Combustible liquids

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

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


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

N6539-25UL:
N6539-200UL:
N6539-BULK:
N6539-VAR:


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試験成績書(COA)

Lot/Batch Number

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以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

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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