Comparison

CASP1 Peptide - middle region (AAP58983)

Item no. AAP58983
Manufacturer AVIVA Systems Biology
Amount 100ug
Category
Type Peptides
Format Lyophilized powder
Applications WB
Specific against Human
ECLASS 10.1 32160409
ECLASS 11.0 32160409
UNSPSC 12352202
Alias ICE, IL1BC, P45
Similar products CASP1
Available
Description
This is a synthetic peptide designed for use in combination with anti-CASP1 Antibody(ARP58983_P050), made by Aviva Systems Biology. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
Gene symbol
CASP1
Protein size
383
Molecular weight
10kDa
Product format
Lyophilized powder
Gene id
834
Reconstitution and storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20C. Avoid repeat freeze-thaw cycles.
Partner proteins
AR, ATN1, ATXN3, HTT, PSEN1, AR, ATN1, ATXN3, BCAP31, BCL2L1, BID, CARD16, CARD17, CARD8, CASP1, CASP14, CAST, CDK11A, CDK11B, EGFR, HTT, IL18, IL1B, LMNA, MAPT, NEDD4, NFE2L2, NLRC4, NLRP1, NOD1, PAK1, PARK2, PARP1, PLA2G4A, PSEN1, PSEN2, PYCARD, RIPK2, TFAP2A, BCAP31, CARD8, CASP1, CASP10, CASP1
Description of target
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.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100ug
Available: In stock
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