p63 Rabbit Monoclonal Antibody【50ul/100ul买二送一】

p63 Rabbit Monoclonal Antibody【50ul/100ul买二送一】

Cat: AMRe21171
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):TP63 KET P63 P73H P73L TP73L

分类: 兔单克隆抗体 标签: , , , , , , , , ,

说明书 复制

产品概述

产品名称(Product Name)

p63 Rabbit Monoclonal Antibody

描述(Description)

Recombinant rabbit monoclonal antibody

宿主(Host)

Rabbit

应用(Application)

WB,IHC,ICC/IF,ELISA,IP

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%protective protein

纯化方式(Purification)

Protein A

 

免疫原

基因名(Gene Name)

TP63

别名(Alternative Names)

KET P63 P73H P73L TP73L

基因ID(Gene ID)

8626

蛋白ID(SwissProt ID)

Q9H3D4

 

产品应用

稀释比(Dilution Ratio)

WB 1:2000-1:10000,IHC 1:1000-1:4000,ICC/IF 1:200-1:1000,ELISA 1:5000-1:20000,IP 1:50-1:200

蛋白分子量(Molecular Weight)

Calculated MW:77kD;Observed MW:77kD

 

研究背景

Cell localization:Nucleus.tumor protein p63(TP63) Homo sapiens This gene encodes a member of the p53 family of transcription factors. The functional domains of p53 family proteins include an N-terminal transactivation domain, a central DNA-binding domain and an oligomerization domain. Alternative splicing of this gene and the use of alternative promoters results in multiple transcript variants encoding different isoforms that vary in their functional properties. These isoforms function during skin development and maintenance, adult stem/progenitor cell regulation, heart development and premature aging. Some isoforms have been found to protect the germline by eliminating oocytes or testicular germ cells that have suffered DNA damage. Mutations in this gene are associated with ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3); split-hand/foot malformation 4 (SHFM4); ankyloblepharon-ectodermal defects-cleft lip/palate; ADULT syndrome (acro-dermato-ungual-lacrim

 

研究领域


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