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WB analysis of Wild-type (WT) and Caspase 8 knockout (KO) HeLa cell extracts using GTX01015 Caspase 8 antibody [GT1152]. Dilution : 1:1000 Loading : 25microg
WB analysis of Wild-type (WT) and Caspase 8 knockout (KO) HeLa cell extracts using GTX01015 Caspase 8 antibody [GT1152]. Dilution : 1:1000 Loading : 25microg
WB analysis of Wild-type (WT) and Caspase 8 knockout (KO) HeLa cell extracts using GTX01015 Caspase 8 antibody [GT1152]. Dilution : 1:1000 Loading : 25microg

Caspase 8 antibody [GT1152] - Recombinant antibody, KO/KD Validated

Research Use Only
GTX01015
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetCASP8
Price on request
Packing Size
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Overview

  • Supplier
    GeneTex
  • Product Name
    Caspase 8 antibody [GT1152] - Recombinant antibody, KO/KD Validated
  • Delivery Days Customer
    9
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    GT1152
  • Conjugate
    Unconjugated
  • Gene ID841
  • Target name
    CASP8
  • Target description
    caspase 8
  • Target synonyms
    ALPS2B; apoptotic cysteine protease; apoptotic protease Mch-5; CAP4; Casp-8; caspase 8, apoptosis-related cysteine peptidase; caspase 8, apoptosis-related cysteine protease; caspase-8; FADD-homologous ICE/CED-3-like protease; FADD-like ICE; FLICE; ICE-like apoptotic protease 5; MACH; MACH-alpha-1/2/3 protein; MACH-beta-1/2/3/4 protein; MCH5; MORT1-associated ced-3 homolog
  • Host
    Rabbit
  • Isotype
    IgG
  • Scientific Description
    This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes composed of a prodomain, a large protease subunit, and a small protease subunit. Activation of caspases requires proteolytic processing at conserved internal aspartic residues to generate a heterodimeric enzyme consisting of the large and small subunits. This protein is involved in the programmed cell death induced by Fas and various apoptotic stimuli. The N-terminal FADD-like death effector domain of this protein smicroggests that it may interact with Fas-interacting protein FADD. This protein was detected in the insoluble fraction of the affected brain region from Huntington disease patients but not in those from normal controls, which implicated the role in neurodegenerative diseases. Many alternatively spliced transcript variants encoding different isoforms have been described, althomicrogh not all variants have had their full-length sequences determined. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human
  • Storage Instruction
    2°C to 8°C,-20°C or -80°C
  • UNSPSC
    12352203