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)

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)

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)

IHC 1:200-1:1000;WB 1:2000-1:10000;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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