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Home All anti-CASP3 antibodies

Anti-CASP3 Antibody E87

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA300366
  • Rabbit Monoclonal Antibody against CASP3 (Clone E87)
  • FREE positive control: HEK293T cell transient overexpression lysate (LC403215) , 20ug
100µl $325 In Stock Add to Shopping Cart
WB(1)
IHC(1)
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Also for CASP3 (NM_032991)
cDNA Clone shRNA/siRNA Protein/Lysate Antibody Assay
Gene NameHomo sapiens caspase 3, apoptosis-related cysteine peptidase (CASP3), transcript variant beta
Synonyms:CPP32; CPP32B; SCA-1
ImmunogenA synthetic peptide corresponding to residues in p17 subunit of human Caspase-3 was used as immunogen. The antibody should recognize both pro-form (35kDa) and p17 cleaved-form of Caspase-3.
Buffer50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA.
Clone NameE87 IsotypeIgG
Species ReactivityHuman, Rat Concentration
Guaranteed Application *WB, IHC Suggested DilutionsWB: 1:5,000; IHC: 1:25-1:50; ICC: 1:25; FC: 1: 10
BackgroundCaspases are a family of cytosolic aspartate-specific cysteine proteases involved in the initiation and execution of apoptosis. Caspase-3 (apopain, SCA-1, Yama and CPP32) is a member of the apoptosis execution functional group of caspases, and is either partially or totally responsible for the proteolytic cleavage of many key proteins during apoptosis, such as poly (ADP-ribose) polymerase (PARP) (1,2,3). Caspase-3 is a cytosolic protein found in cells as an inactive 32 kDa proenzyme. It is activated by proteolytic cleavage into two active subunits only when cells undergo apoptosis (3).
Related Pathway
Apoptosis
MAPK signaling pathway

* Shipping is in business days
* OriGene provides validated application data and protocol, with money back guarantee.

WB Image
Western blot analysis on (1) Jurkat and (2) Camptothecin-treated Jurkat cell lysates using anti-Caspase-3, 1:5,000 dilution.
IHC Image
Immunohistochemical analysis of paraffin-embedded cervical carcinoma using anti-Caspase-3.

 

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