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SEC23IP 抗体 (AA 30-426)

The 兔 多克隆 anti-SEC23IP antibody is suitable to detect SEC23IP in samples from 人, 小鼠, 大鼠 和 猴. It has been validated for WB, ELISA, IF, IHC (p) 和 FACS.
产品编号 ABIN7873584
发货至: 中国
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Quick Overview for SEC23IP 抗体 (AA 30-426) (ABIN7873584)

抗原

See all SEC23IP 抗体
SEC23IP (SEC23 Interacting Protein (SEC23IP))

适用

  • 34
  • 9
  • 9
  • 6
  • 6
  • 5
  • 5
  • 5
  • 2
  • 2
  • 2
人, 小鼠, 大鼠, 猴

宿主

  • 30
  • 4

克隆类型

  • 33
  • 1
多克隆

标记

  • 25
  • 3
  • 2
  • 2
  • 1
  • 1
This SEC23IP antibody is un-conjugated

应用范围

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  • 13
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  • 3
  • 3
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  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • 抗原表位

    • 9
    • 5
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 30-426

    原理

    SEC23IP Antibody / SEC23-interacting protein

    纯化方法

    Antigen affinity purified

    免疫原

    E. coli-derived recombinant human protein (amino acids E30-R426) was used as the immunogen for the SEC23IP antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the SEC23IP antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the SEC23IP antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    SEC23IP (SEC23 Interacting Protein (SEC23IP))

    别名

    SEC23IP

    背景

    SEC23-interacting protein is a protein that in humans is encoded by the SEC23IP gene. This gene encodes a member of the phosphatidic acid preferring-phospholipase A1 family. The encoded protein is localized to endoplasmic reticulum exit sites and plays a critical role in ER-Golgi transport as part of the multimeric coat protein II complex. An orthologous gene in frogs is required for normal neural crest cell development, suggesting that this gene may play a role in Waardenburg syndrome neural crest defects. Alternatively spliced transcript variants have been observed for this gene.

    UniProt

    Q9Y6Y8
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