Notch1 Rabbit Monoclonal antibody

Notch1 Rabbit Monoclonal antibody

规格:50μL 价格:¥1500
规格:100μL 价格:¥2400
应用(Application):WB,IHC,IF,IP,ELISA

种属(Reactivity):Human,Mouse,Rat,
偶联物(Conjugate):Unconjugated
基因名(Gene Name):NOTCH1
SKU: AMRe21558 Category: 兔单克隆抗体 Tags: , , , , , , , , ,

说明书 复制

产品概述

产品名称(Product Name)

Notch1 Rabbit Monoclonal antibody

描述(Description)

Rabbit Monoclonal antibody

宿主(Host)

Rabbit

应用(Application)

WB,IHC,IF,IP,ELISA

种属反应性(Reactivity)

Human,Mouse,Rat,

 

产品性能

偶联物(Conjugation)

Unconjugated

修饰(Modification)

Unmodified

同种型(Isotype)

IgG,Kappa

克隆(Clonality)

Monoclonal

形式(Form)

Liquid

存放说明(Storage)

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

储存溶液(Buffer)

PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

纯化方式(Purification)

Protein A

 

免疫原

基因名(Gene Name)

NOTCH1

别名(Alternative Names)

NOTCH1;TAN1;Neurogenic locus notch homolog protein 1;Notch 1;hN1;Translocation-associated notch protein TAN-1

基因ID(Gene ID)

4851

蛋白ID(SwissProt ID)

P46531

 

产品应用

稀释比(Dilution Ratio)

IHC 1:200-1000;WB 1:1000-5000;IF 1:200-1000;ELISA 1:5000-20000;IP 1:50-200

蛋白分子量(Molecular Weight)

Calculated MW:273kD;Observed MW:120kD

 

研究背景

Cell localization:Membranous.notch 1(NOTCH1) Homo sapiens This gene encodes a member of the NOTCH family of proteins. Members of this Type I transmembrane protein family share structural characteristics including an extracellular domain consisting of multiple epidermal growth factor-like (EGF) repeats, and an intracellular domain consisting of multiple different domain types. Notch signaling is an evolutionarily conserved intercellular signaling pathway that regulates interactions between physically adjacent cells through binding of Notch family receptors to their cognate ligands. The encoded preproprotein is proteolytically processed in the trans-Golgi network to generate two polypeptide chains that heterodimerize to form the mature cell-surface receptor. This receptor plays a role in the development of numerous cell and tissue types. Mutations in this gene are associated with aortic valve disease, Adams-Oliver syndrome, T-cell acute lymphoblastic leukemia, chronic lymph

 

研究领域


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