SCP2 (Human) IP-WB Antibody Pair

Catalog # H00006342-PW1

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Size:1 Set
Price: USD $ 607.00
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Immunoprecipitation of SCP2 transfected lysate using mouse monoclonal anti-SCP2 and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-SCP2.

  • 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

    Quality Control Testing

    Immunoprecipitation-Western Blot (IP-WB)

    Immunoprecipitation of SCP2 transfected lysate using mouse monoclonal anti-SCP2 and Protein A Magnetic Bead (U0007), and immunoblotted with rabbit polyclonal anti-SCP2.

    Supplied Product

    Antibody pair set content:
    1. Antibody pair for IP: mouse monoclonal anti-SCP2 (300 ug)
    2. Antibody pair for WB: rabbit polyclonal anti-SCP2 (50 ul)

    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 — SCP2

    Entrez GeneID

    6342

    Gene Name

    SCP2

    Gene Alias

    DKFZp686C12188, DKFZp686D11188, NLTP, NSL-TP, SCPX

    Gene Description

    sterol carrier protein 2

    Omim ID

    184755

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2), as a result of transcription initiation from 2 independently regulated promoters. The transcript initiated from the proximal promoter encodes the longer SCPx protein, and the transcript initiated from the distal promoter encodes the shorter SCP2 protein, with the 2 proteins sharing a common C-terminus. Evidence suggests that the SCPx protein is a peroxisome-associated thiolase that is involved in the oxidation of branched chain fatty acids, while the SCP2 protein is thought to be an intracellular lipid transfer protein. This gene is highly expressed in organs involved in lipid metabolism, and may play a role in Zellweger syndrome, in which cells are deficient in peroxisomes and have impaired bile acid synthesis. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms. The full-length nature of all transcript variants has not been determined. [provided by RefSeq

    Other Designations

    OTTHUMP00000010488|nonspecific lipid-transfer protein|sterol carrier protein X

  • 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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