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NSDHL 抗体 (AA 7-373) (FITC)

This 兔 多克隆 antibody specifically detects NSDHL in FACS. It exhibits reactivity toward 人, 大鼠 和 小鼠.
产品编号 ABIN8013365
发货至: 中国
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Room 801-803
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Quick Overview for NSDHL 抗体 (AA 7-373) (FITC) (ABIN8013365)

抗原

See all NSDHL 抗体
NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))

适用

  • 58
  • 29
  • 26
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 大鼠, 小鼠

宿主

  • 54
  • 4

克隆类型

  • 29
  • 29
多克隆

标记

  • 27
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NSDHL antibody is conjugated to FITC

应用范围

  • 47
  • 22
  • 17
  • 16
  • 15
  • 13
  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS)
  • 抗原表位

    • 12
    • 6
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 7-373

    原理

    Anti-NSDHL Antibody FITC Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins

    预测反应

    Human NSDHL shares 83.4%,87.3% amino acid (aa) sequence identity with mouse,rat NSDHL,respectively.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human NSDHL recombinant protein (Position: E7-K373). Human NSDHL shares 83.4% and 87.3% amino acid (aa) sequence identity with mouse and rat NSDHL, respectively.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, 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, 0.02 % Sodium azide.

    储存液

    Sodium azide

    注意事项

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

    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. Protect from light.

    有效期

    12 months
  • 抗原

    NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))

    别名

    NSDHL

    背景

    Background: The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene.

    Gene Full Name: NAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL

    基因ID

    50814

    UniProt

    Q15738
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