CASP12 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-15533
Catalog Number: E-AB-15533
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: WB,IHC,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: WB,IHC,ELISA
Datasheet, Questions? Contact us!
Background:
Caspases are cysteine proteases that cleave C-terminal aspartic acid residues on their substrate molecules. This gene is most highly related to members of the ICE subfamily of caspases that process inflammatory cytokines. In rodents, the homolog of this gene mediates apoptosis in response to endoplasmic reticulum stress. However, in humans this gene contains a polymorphism for the presence or absence of a premature stop codon. The majority of human individuals have the premature stop codon and produce a truncated non-functional protein. The read-through codon occurs primarily in individuals of African descent and carriers have endotoxin hypo-responsiveness and an increased susceptibility to severe sepsis. Several alternatively spliced transcript variants have been noted for this gene.
Research Area: Cancer, Cell Biology, Metabolism, Neuroscience
Synonyms:
CASP 12, CASP-12, Casp12, CASP12P1, caspase 12 (gene/pseudogene), caspase 12 pseudogene 1, CASPC, Inactive caspase-12, OTTHUMP00000207032
Immunogen: Synthetic peptide of human CASP12
Swissprot: Q6UXS9
Gene Accession: NP_001177945
Calculated MW: 55 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.4 mg/mL
Dilution: WB 1:500-1:2000, IHC 1:50-1:200
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-12395/sc-12396/sc-5627
Caspases are cysteine proteases that cleave C-terminal aspartic acid residues on their substrate molecules. This gene is most highly related to members of the ICE subfamily of caspases that process inflammatory cytokines. In rodents, the homolog of this gene mediates apoptosis in response to endoplasmic reticulum stress. However, in humans this gene contains a polymorphism for the presence or absence of a premature stop codon. The majority of human individuals have the premature stop codon and produce a truncated non-functional protein. The read-through codon occurs primarily in individuals of African descent and carriers have endotoxin hypo-responsiveness and an increased susceptibility to severe sepsis. Several alternatively spliced transcript variants have been noted for this gene.
Research Area: Cancer, Cell Biology, Metabolism, Neuroscience
Synonyms:
CASP 12, CASP-12, Casp12, CASP12P1, caspase 12 (gene/pseudogene), caspase 12 pseudogene 1, CASPC, Inactive caspase-12, OTTHUMP00000207032
Immunogen: Synthetic peptide of human CASP12
Swissprot: Q6UXS9
Gene Accession: NP_001177945
Calculated MW: 55 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.4 mg/mL
Dilution: WB 1:500-1:2000, IHC 1:50-1:200
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-12395/sc-12396/sc-5627
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