CTSC 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00001075-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

CTSC transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: CTSC transfected lysate ( 51.8 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-CTSC full-length

    Host

    Human

    Theoretical MW (kDa)

    51.8

    Interspecies Antigen Sequence

    Mouse (78); Rat (80)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-CTSC antibody (H00001075-B01) by Western Blots.

    SDS-PAGE Gel

    CTSC transfected lysate.

    Western Blot

    Lane 1: CTSC transfected lysate ( 51.8 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 — CTSC

    Entrez GeneID

    1075

    GeneBank Accession#

    NM_001814

    Protein Accession#

    NP_001805

    Gene Name

    CTSC

    Gene Alias

    CPPI, DPP1, DPPI, HMS, JP, JPD, PALS, PLS

    Gene Description

    cathepsin C

    Omim ID

    170650 245000 245010 602365

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene, a member of the peptidase C1 family, is a lysosomal cysteine proteinase that appears to be a central coordinator for activation of many serine proteinases in immune/inflammatory cells. It is composed of a dimer of disulfide-linked heavy and light chains, both produced from a single protein precursor, and a residual portion of the propeptide acts as an intramolecular chaperone for the folding and stabilization of the mature enzyme. This enzyme requires chloride ions for activity and can degrade glucagon. Defects in the encoded protein have been shown to be a cause of Papillon-Lefevre syndrome, an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    cathepsin J|dipeptidyl transferase|dipeptidyl-peptidase I

  • 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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