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GLT8D1 抗体 (FITC)

This anti-GLT8D1 antibody is a 兔 多克隆 antibody detecting GLT8D1 in WB 和 IF (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1403402
发货至: 中国

Quick Overview for GLT8D1 抗体 (FITC) (ABIN1403402)

抗原

See all GLT8D1 抗体
GLT8D1 (Glycosyltransferase 8 Domain Containing 1 (GLT8D1))

适用

  • 36
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  • 2
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  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 36

克隆类型

  • 36
多克隆

标记

  • 13
  • 3
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  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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This GLT8D1 antibody is conjugated to FITC

应用范围

  • 31
  • 14
  • 12
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human GLT8D1

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200

    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.

    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

    GLT8D1 (Glycosyltransferase 8 Domain Containing 1 (GLT8D1))

    别名

    GLT8D1

    背景

    Synonyms: MGC94018, Da2 24, GALA4A, Glycosyltransferase 8 domain containing 1, Glycosyltransferase 8 domain-containing protein 1, Glycosyltransferase AD 017, MSTP139, GL8D1_HUMAN.

    Background: GLT8D1 is a 371 amino acid single-pass type II transmembrane protein that is expressed by a gene residing on human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. There are two isoforms of GLT8D1 that are produced as a result of alternative splicing events.

    基因ID

    55830
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