COCH 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00001690-T01

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Size:100 uL
Price: USD $ 247.00
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Contact Info
  • +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

COCH transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: COCH transfected lysate ( 53.2 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-COCH full-length

    Host

    Human

    Theoretical MW (kDa)

    53.2

    Interspecies Antigen Sequence

    Mouse (95)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-COCH antibody (H00001690-B01) by Western Blots.

    SDS-PAGE Gel

    COCH transfected lysate.

    Western Blot

    Lane 1: COCH transfected lysate ( 53.2 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 — COCH

    Entrez GeneID

    1690

    GeneBank Accession#

    BC007230

    Protein Accession#

    AAH07230

    Gene Name

    COCH

    Gene Alias

    COCH-5B2, COCH5B2, DFNA9

    Gene Description

    coagulation factor C homolog, cochlin (Limulus polyphemus)

    Omim ID

    601369 603196

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94% and 79% amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated. [provided by RefSeq

    Other Designations

    cochlin

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