hPL Mouse Monoclonal Antibody

hPL Mouse Monoclonal Antibody

Cat: AMM22003
规格:50μL 价格:¥1200
规格:100μL 价格:¥2150
应用(Application):IHC,IF,ELISA

种属(Reactivity):Human
偶联物(Conjugate):Unconjugated
基因名(Gene Name):CSH1/CSH2

分类: 病理IHC抗体 标签: , , , , , ,

说明书 复制

产品概述

产品名称(Product Name)

hPL Mouse Monoclonal Antibody

描述(Description)

病理IHC抗体

宿主(Host)

Mouse

应用(Application)

IHC,IF,ELISA

种属反应性(Reactivity)

Human

 

产品性能

偶联物(Conjugation)

Unconjugated

修饰(Modification)

Unmodified

同种型(Isotype)

IgG2b,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)

The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.

 

免疫原

基因名(Gene Name)

CSH1/CSH2

别名(Alternative Names)

PL;CSB;CS-2;GHB1;hCS-B;CSA;CS-1;CSMT;GHB3;hCS-1;hCS-A

基因ID(Gene ID)

Human:1442

蛋白ID(SwissProt ID)

Human:P0DML2;P0DML3

 

产品应用

稀释比(Dilution Ratio)

IHC 1:200-400;IF 1:50-200;ELISA 1:500-5000

蛋白分子量(Molecular Weight)

Observed MW:25kDa

 

研究背景

The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. The gene is located at the growth hormone locus on chromosome 17 along with four other related genes in the same transcriptional orientation; an arrangement which is thought to have evolved by a series of gene duplications. Although the five genes share a remarkably high degree of sequence identity, they are expressed selectively in different tissues. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. This particular family member is expressed mainly in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, although the ratio of 1 to 2 increases by term. Mutations in this gene result in placental lactogen deficiency and Silver-Russell syndrome. [provided by RefSeq, Jul 2008]

 

研究领域

Pathology


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