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SOGA2 抗体 (AA 884-1522) (HRP)

The 兔 多克隆 anti-SOGA2 antibody is suitable to detect SOGA2 in samples from 人, 小鼠 和 大鼠. It has been validated for WB, ELISA 和 IHC.
产品编号 ABIN8038785
发货至: 中国
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Quick Overview for SOGA2 抗体 (AA 884-1522) (HRP) (ABIN8038785)

抗原

SOGA2 (SOGA Family Member 2 (SOGA2))

适用

人, 小鼠, 大鼠

宿主

  • 19

克隆类型

  • 19
多克隆

标记

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SOGA2 antibody is conjugated to HRP

应用范围

  • 11
  • 10
  • 8
  • 4
  • 2
  • 2
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • 抗原表位

    • 12
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 884-1522

    原理

    Anti-MTCL1 Antibody HRP Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human MTCL1 recombinant protein (Position: K884-D1522).

    亚型

    IgG
  • 应用备注

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    SOGA2 (SOGA Family Member 2 (SOGA2))

    别名

    MTCL1

    背景

    Background: MTCL1 (microtubule cross-linking factor 1), also known as CCDC165 (Coiledcoil domain-containing protein 165), SOGA2 or MTCL1, is a 1,905 amino acid protein that localizes to the cell membrane, cytoplasm and cytoskeleton. MTCL1 is a microtubule-associated factor that plays a role in regulating polarization and microtubule dynamics as well as the development and maintenance of non-centrosomal microtubule bundles. MTCL1 is encoded by a gene that maps to chromosome 18 and is expressed as four isoforms due to alternative splicing events. Chromosome 18 encodes over 300 genes and contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGFβ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.

    Gene Full Name: microtubule crosslinking factor 1

    基因ID

    23255

    UniProt

    Q9Y4B5
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