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DHCR7 抗体 (C-Term)

This anti-DHCR7 antibody is a 兔 多克隆 antibody detecting DHCR7 in WB, IF 和 IHC (p). Suitable for 人 和 小鼠.
产品编号 ABIN655399
发货至: 中国

Quick Overview for DHCR7 抗体 (C-Term) (ABIN655399)

抗原

See all DHCR7 抗体
DHCR7 (7-Dehydrocholesterol Reductase (DHCR7))

适用

  • 37
  • 31
  • 14
人, 小鼠

宿主

  • 41
  • 2

克隆类型

  • 41
  • 2
多克隆

标记

  • 15
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DHCR7 antibody is un-conjugated

应用范围

  • 33
  • 15
  • 14
  • 9
  • 9
  • 5
  • 5
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

克隆位点

RB17942
  • 抗原表位

    • 7
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 437-463, C-Term

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This DHCR7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 437-463 amino acids from the C-terminal region of human DHCR7.

    亚型

    Ig Fraction
  • 应用备注

    IF: 1:25. IF: 1:10~50. WB: 1:2000. WB: 1:1000. IHC-P: 1:50~100

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    DHCR7 (7-Dehydrocholesterol Reductase (DHCR7))

    别名

    DHCR7

    背景

    This gene encodes an enzyme that removes the C(7-8) double bond in the B ring of sterols and catalyzes the conversion of 7-dehydrocholesterol to cholesterol. This gene is ubiquitously expressed and its transmembrane protein localizes to the endoplasmic reticulum membrane and nuclear outer membrane. Mutations in this gene cause Smith-Lemli-Opitz syndrome (SLOS), a syndrome that is metabolically characterized by reduced serum cholesterol levels and elevated serum 7-dehydrocholesterol levels and phenotypically characterized by mental retardation, facial dysmorphism, syndactyly of second and third toes, and holoprosencephaly in severe cases to minimal physical abnormalities and near-normal intelligence in mild cases. Alternative splicing results in multiple transcript variants that encode the same protein.

    分子量

    54489

    基因ID

    1717

    NCBI登录号

    NP_001157289, NP_001351

    UniProt

    Q9UBM7
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