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DHCR7 抗体 (AA 437-463)

This 兔 多克隆 antibody specifically detects DHCR7 in WB, IF 和 IHC (p). It exhibits reactivity toward 人 和 小鼠.
产品编号 ABIN7874996
发货至: 中国
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Quick Overview for DHCR7 抗体 (AA 437-463) (ABIN7874996)

抗原

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

适用

  • 37
  • 33
  • 14
人, 小鼠

宿主

  • 42
  • 1

克隆类型

  • 42
  • 1
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
  • 14
  • 12
  • 10
  • 8
  • 6
  • 4
  • 1
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 8
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 437-463

    原理

    DHCR7 Antibody / 7-dehydrocholesterol reductase

    纯化方法

    Antigen affinity purified

    免疫原

    A portion of amino acids 437-463 from the human protein was used as the immunogen for the DHCR7 antibody.

    亚型

    Ig Fraction
  • 应用备注

    The stated application concentrations are suggested starting points. Titration of the DHCR7 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    In 1X PBS, pH 7.4, with 0.09 % 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

    Aliquot the DHCR7 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 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.

    UniProt

    Q9UBM7
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