OCLN Rabbit Monoclonal Antibody

OCLN 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):OCLN
SKU: AMRe21373 Category: 兔单克隆抗体 Tags: , , , , , , , , ,

说明书 复制

产品概述

产品名称(Product Name)

OCLN 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)

OCLN

别名(Alternative Names)

基因ID(Gene ID)

100506658

蛋白ID(SwissProt ID)

Q16625

 

产品应用

稀释比(Dilution Ratio)

WB 1:2000-1:10000,IHC 1:200-1:1000,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:59kD;Observed MW:65kD

 

研究背景

Cell localization:Membrane.This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011],

 

研究领域


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