Bio-Connect
WB analysis of HeLa (A) and NIH-3T3 (B) cell lysate using GTX14367 Caspase 1 antibody [14F468]. Dilution : 0.5 microg/ml and 2 microg/ml
WB analysis of HeLa (A) and NIH-3T3 (B) cell lysate using GTX14367 Caspase 1 antibody [14F468]. Dilution : 0.5 microg/ml and 2 microg/ml
WB analysis of HeLa (A) and NIH-3T3 (B) cell lysate using GTX14367 Caspase 1 antibody [14F468]. Dilution : 0.5 microg/ml and 2 microg/ml

Caspase 1 antibody [14F468]

GTX14367
GeneTex
ApplicationsFlow Cytometry, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetCASP1
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    Caspase 1 antibody [14F468]
  • Delivery Days Customer
    9
  • Antibody Specificity
    The antibody will recognize full-length Caspase-1 and cleaved caspase-1 forms that retain amino acids 371-390 of the Caspase-1 protein.
  • Application Supplier Note
    WB: 0.5 - 2 microg/ml. IHC-P: 1:10 - 1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    14F468
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID834
  • Target name
    CASP1
  • Target description
    caspase 1
  • Target synonyms
    CASP1 nirs variant 1; caspase 1, apoptosis-related cysteine peptidase; caspase-1; caspase-1 isoform alpha; ICE; IL-1 beta-converting enzyme; IL1BC; IL1B-convertase; interleukin 1, beta, convertase; interleukin 1-B converting enzyme; P45
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP29466
  • Protein Name
    Caspase-1
  • Scientific Description
    This gene encodes a protein which is 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 which undergo proteolytic processing at conserved aspartic residues to produce 2 subunits, large and small, that dimerize to form the active enzyme. This gene was identified by its ability to proteolytically cleave and activate the inactive precursor of interleukin-1, a cytokine involved in the processes such as inflammation, septic shock, and wound healing. This gene has been shown to induce cell apoptosis and may function in various developmental stages. Studies of a similar gene in mouse suggest a role in the pathogenesis of Huntington disease. Alternative splicing of this gene results in five transcript variants encoding distinct isoforms. [provided by RefSeq]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Biejiajian Pill Ameliorates Diabetes-Associated Atherosclerosis through Inhibition of the NLRP3 Inflammasome. Fu Y et al., 2022, Evid Based Complement Alternat Med
    Read more
  • TRIM28 SUMOylates and stabilizes NLRP3 to facilitate inflammasome activation. Qin Y et al., 2021 Aug 9, Nat Commun
    Read more
  • Long Non-coding RNA MEG3 Promotes Renal Tubular Epithelial Cell Pyroptosis by Regulating the miR-18a-3p/GSDMD Pathway in Lipopolysaccharide-Induced Acute Kidney Injury. Deng J et al., 2021, Front Physiol
    Read more
  • UAF1 deubiquitinase complexes facilitate NLRP3 inflammasome activation by promoting NLRP3 expression. Song H et al., 2020 Nov 27, Nat Commun
    Read more
  • Periodontal inflammation recruits distant metastatic breast cancer cells by increasing myeloid-derived suppressor cells. Cheng R et al., 2020 Feb, Oncogene
    Read more
  • Histone deacetylase inhibitors mediate DNA damage repair in ameliorating hemorrhagic cystitis. Haldar S et al., 2016 Dec 20, Sci Rep
    Read more
  • Obesity-associated NLRC4 inflammasome activation drives breast cancer progression. Kolb R et al., 2016 Oct 6, Nat Commun
    Read more