Dopamine β-Hydroxylase (DBH) Antibody

Dopamine β-Hydroxylase (DBH) A

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月13日
  • W
  • Rabbit
  • H
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    • 详细信息
    • 技术资料
    • 抗体英文名

      Dopamine β-Hydroxylase (DBH) Antibody

    • 抗原

      synthetic peptide corresponding to residues surrounding Ala211 of human dopamine β-hydroxylase protein

    • 应用范围

      W

    • 宿主

      Rabbit

    • 库存

      大量

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 适应物种

      H

    • 是否单克隆

      2

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Source
    W H Endogenous 75-80 Rabbit
    Protocols
    Specificity / Sensitivity

    Dopamine β-Hydroxylase (DBH) Antibody recognizes endogenous levels of total DBH protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala211 of human dopamine β-hydroxylase protein. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from SH-SY5Y cells, untreated (-) or treated with TPA (200 nM, 24 hr) #4174 (+), and 293 cells, using Dopamine β-Hydroxylase (DBH) Antibody.

    Background

    Dopamine β-Hydroxylase (DBH) is an enzyme of the copper type II ascorbate-dependent mono-oxygenase family. This enzyme forms homotetramers composed of two noncovalently bound disulfide-linked dimers and is found as both membrane-associated and soluble forms (1-3). The soluble form is present in the lumen of secretory granules (4) and is released from cells by exocytosis (5). DBH converts dopamine to noradrenaline (6). Deficiency in this enzyme causes a rare disease characterized by a complete absence of noradrenaline and adrenaline in plasma together with increased plasma dopamine levels (7). Orthostatic hypotension, the main symptom of DBH deficiency, can be alleviated by administration of dihydroxyphenylserine, a synthetic precursor of noradrenaline (8).

    1. Smith, W.J. and Kirshner, N. (1967) Mol Pharmacol 3, 52-62.
    2. Lagercrantz, H. (1976) Neuroscience 1, 81-92.
    3. Winkler, H. (1976) Neuroscience 1, 65-80.
    4. Laduron, P.M. (1975) FEBS Lett 52, 132-4.
    5. Weinshilboum, R.M. et al. (1971) Science 174, 1349-51.
    6. Kaufman, S. and Friedman, S. (1965) Pharmacol Rev 17, 71-100.
    7. Robertson, D. et al. (1986) N Engl J Med 314, 1494-7.
    8. Biaggioni, I. and Robertson, D. (1987) Lancet 2, 1170-2.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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