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GLCCI1 抗体 (AA 201-300) (HRP)

This anti-GLCCI1 antibody is a 兔 多克隆 antibody detecting GLCCI1 in WB, ELISA, IHC (p) 和 IHC (fro). Suitable for 小鼠.
产品编号 ABIN1416796
发货至: 中国

Quick Overview for GLCCI1 抗体 (AA 201-300) (HRP) (ABIN1416796)

抗原

See all GLCCI1 抗体
GLCCI1 (Glucocorticoid Induced Transcript 1 (GLCCI1))

适用

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小鼠

宿主

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克隆类型

  • 45
多克隆

标记

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This GLCCI1 antibody is conjugated to HRP

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 抗原表位

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    AA 201-300

    交叉反应

    小鼠

    预测反应

    Human,Rat,Dog,Cow,Sheep,Horse,Chicken

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human GLCCI1

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    注意事项

    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    GLCCI1 (Glucocorticoid Induced Transcript 1 (GLCCI1))

    别名

    GLCCI1

    背景

    Synonyms: FAM117C, GIG18, GLCCI1, GLCI1_HUMAN, Glucocorticoid induced transcript 1, Glucocorticoid-induced transcript 1 protein, TSSN1.

    Background: GLCCI1, also known as TSSN1, GIG18 or FAM117C, is a 547 amino acid protein found in thymus and CD4(+)CD8(+) cells during specific stages of spermatogenesis in testis. Subject to phosphorylation, GLCCI1 is encoded by a gene located on human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

    基因ID

    113263
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