COX10 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00001352-T01

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Size:100 uL
Price: USD $ 247.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

COX10 transfected lysate

Western Blot
QC Test

Western Blot

Lane 1: COX10 transfected lysate ( 48.73 KDa).
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-COX10 full-length

    Host

    Human

    Theoretical MW (kDa)

    48.73

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-COX10 antibody (H00001352-B01) by Western Blots.

    SDS-PAGE Gel

    COX10 transfected lysate

    Western Blot

    Lane 1: COX10 transfected lysate ( 48.73 KDa).
    Lane 2: Non-transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — COX10

    Entrez GeneID

    1352

    GeneBank Accession#

    BC006394

    Protein Accession#

    AAH06394

    Gene Name

    COX10

    Gene Alias

    -

    Gene Description

    COX10 homolog, cytochrome c oxidase assembly protein, heme A: farnesyltransferase (yeast)

    Omim ID

    602125

    Gene Ontology

    Hyperlink

    Gene Summary

    Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes heme A:farnesyltransferase, which is not a structural subunit but required for the expression of functional COX and functions in the maturation of the heme A prosthetic group of COX. This protein is predicted to contain 7-9 transmembrane domains localized in the mitochondrial inner membrane. A gene mutation, which results in the substitution of a lysine for an asparagine (N204K), is identified to be responsible for cytochrome c oxidase deficiency. In addition, this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion. [provided by RefSeq

    Other Designations

    cytochrome c oxidase assembly protein|cytochrome c oxidase subunit X|heme A: farnesyltransferase|heme A:farnesyltransferase

  • 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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