CYP27A1 (Human) IP-WB Antibody Pair

Catalog # H00001593-PW1

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Size:1 Set
Price: USD $ 607.00
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Immunoprecipitation of CYP27A1 transfected lysate using rabbit polyclonal anti-CYP27A1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-CYP27A1.

  • Specification

    Product Description

    This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (71%); Rat (72%)

    Quality Control Testing

    Immunoprecipitation-Western Blot (IP-WB)

    Immunoprecipitation of CYP27A1 transfected lysate using rabbit polyclonal anti-CYP27A1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-CYP27A1.

    Supplied Product

    Antibody pair set content:
    1. Antibody pair for IP: rabbit polyclonal anti-CYP27A1 (300 ul)
    2. Antibody pair for WB: mouse purified polyclonal anti-CYP27A1 (50 ug)

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    Immunoprecipitation-Western Blot

  • Gene Info — CYP27A1

    Entrez GeneID

    1593

    Gene Name

    CYP27A1

    Gene Alias

    CP27, CTX, CYP27

    Gene Description

    cytochrome P450, family 27, subfamily A, polypeptide 1

    Omim ID

    213700 606530

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein oxidizes cholesterol intermediates as part of the bile synthesis pathway. Since the conversion of cholesterol to bile acids is the major route for removing cholesterol from the body, this protein is important for overall cholesterol homeostasis. Mutations in this gene cause cerebrotendinous xanthomatosis, a rare autosomal recessive lipid storage disease. [provided by RefSeq

    Other Designations

    5-beta-cholestane-3-alpha, 7-alpha, 12-alpha-triol 26-hydroxylase|5-beta-cholestane-3-alpha, 7-alpha, 12-alpha-triol 27-hydroxylase|cholestanetriol 26-monooxygenase|cytochrome P-450C27/25|cytochrome P450, subfamily XXVIIA (steroid 27-hydroxylase, cerebrot

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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