hPL (ABT223) mouse mAb

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¥880.00

市场价:¥1280.00

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产品规格:
  • 50μL
货号:

FAB2602020

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商品描述
  • 靶点-Target

    Humanm Placental lactogen

  • 反应性

    Human,

  • 应用

    IHC,IF,ELISA

  • 宿主物种-Host Species

    Mouse

  • 同种型-Isotype

    IgG2b,Kappa

  • 修饰-Modification

    Unmodified

  • MW(Observed)

    25kD

  • 推荐稀释比

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

  • 组成

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

  • 纯化工艺

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

  • 储存

    -15°C to -25°C/1 year(Do not lower than -25°C)

  • 克隆性

    Monoclonal

  • 克隆号

    ABT223

  • 免疫原

    Synthesized peptide derived from humanSynthesized peptide derived from humanPlacental lactogen AA range:100-200

  • 特异性

    This antibody detects endogenous levels of hPL.

  • 基因名称

    CSH1/CSH2

  • 蛋白名称

    Chorionic somatomammotropin hormone 1/Chorionic somatomammotropin hormone 2

  • 别名

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

  • Organism-1

    Human

  • 基因ID-1

    1442

  • SwissProt-1

    P0DML2;P0DML3

  • 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]

  • 细胞定位

    Cytoplasmic