Caspase 10 (p23/17, Cleaved-Val220) Rabbit pAb

Caspase 10 (p23/17, Cleaved-Val220) Rabbit pAb

AO-06-ES17852-50

Caspase 10 (p23/17, Cleaved-Val220) Rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES17852
Product nameCaspase 10 (p23/17, Cleaved-Val220) Rabbit pAb
ReactivityHuman; Mouse; Rat
ApplicationsWB; ELISA
Other nameCaspase-10 (CASP-10;EC 3.4.22.63;Apoptotic protease Mch-4;FAS-associated death domain protein interleukin-1B-converting enzyme 2;FLICE2;ICE-like apoptotic protease 4) [Cleaved into: Caspase-10 subunit p23/17; Caspase-10 subunit p12]
Size50μL
Unit price ($)148
Human gene ID843
Human Swiss-ProtQ92851
SourceRabbit
IsotypeIgG
TargetCaspase-10
Fields>>Apoptosis;>>RIG-I-like receptor signaling pathway;>>TNF signaling pathway;>>Tuberculosis;>>Hepatitis B
Gene nameCASP10 MCH4
Protein nameCaspase10
Human gene link
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-Prot
Mouse Swiss link
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human Caspase 10 (p23/17, Cleaved-Val220)
SpecificityThis antibody detects endogenous levels of human Caspase 10 (p23/17, Cleaved-Val220)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000, ELISA(peptide)1:5000-20000
PurificationThe antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)58+23kD
BackgroundThis 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 two subunits, large and small, that dimerize to form the active enzyme. This protein cleaves and activates caspases 3 and 7, and the protein itself is processed by caspase 8. Mutations in this gene are associated with type IIA autoimmune lymphoproliferative syndrome, non-Hodgkin lymphoma and gastric cancer. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011],
Functioncatalytic activity:Strict requirement for Asp at position P1 and has a preferred cleavage sequence of Leu-Gln-Thr-Asp-|-Gly.,disease:Defects in CASP10 are a cause of familial non-Hodgkin lymphoma (NHL) [MIM:605027]. NHL is a cancer that starts in cells of the lymph system, which is part of the body's immune system. NHLs can occur at any age and are often marked by enlarged lymph nodes, fever and weight loss.,disease:Defects in CASP10 are a cause of gastric cancers [MIM:137215].,disease:Defects in CASP10 are the cause of autoimmune lymphoproliferative syndrome type 2A (ALPS2A) [MIM:603909]. ALPS2 is characterized by abnormal lymphocyte and dendritic cell homeostasis and immune regulatory defects.,function:Involved in the activation cascade of caspases responsible for apoptosis execution. Recruited to both Fas- and TNFR-1 receptors in a FADD dependent manner. May participate in the granzym
Subcellular locationcytosol,CD95 death-inducing signaling complex,ripoptosome,
ExpressionDetectable in most tissues. Lowest expression is seen in brain, kidney, prostate, testis and colon.

Additional Images

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Western blot analysis of Hela cell treated or untreated with 2 mM/ml camptothecin , primary antibody was diluted at 1:1000, 4° over night, secondary antibody(cat: RS23920)was diluted at 1:10000, 37° 1hour.
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: AO-06-ES17852-50
: 10 Items
Hurry! only 10 items left in stock.

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