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ELK Biotechnology Cleaved-Caspase-1 p20 (N120) rabbit pAb
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ELK Biotechnology Cleaved-Caspase-1 p20 (N120) rabbit pAb

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Cleaved-Caspase-1 p20 (N120) rabbit polyclonal antibody로, 인간, 마우스, 랫트 시료에 반응합니다. Western blot과 ELISA에 적합하며, 세포자멸사 연구에 유용합니다. 합성 펩타이드 면역원으로 제작되었으며, -20°C에서 1년 보관 가능합니다.

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pk
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ELK Biotechnology ES7678-100UL Cleaved-Caspase-1 p20 (N120) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7678-50UL Cleaved-Caspase-1 p20 (N120) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Cleaved-Caspase-1 p20 (N120) rabbit pAb

Cleaved-Caspase-1 p20 (N120) rabbit pAb

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항목 내용
Product Name Cleaved-Caspase-1 p20 (N120) rabbit pAb
Alternative Names CASP1; IL1BC; IL1BCE; Caspase-1; CASP-1; Interleukin-1 beta convertase; IL-1BC; Interleukin-1 beta-converting enzyme; ICE; IL-1 beta-converting enzyme; p45
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/20000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human Caspase 1 (AA range: 101–150)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 20 kDa
Gene ID (Human) 834
Human Swiss-Prot No. P29466
Cellular Localization Cytoplasm, Cell membrane
Species Reactivity Human, Rat, Mouse

Background

This gene encodes a protein that belongs to 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 that undergo proteolytic processing at conserved aspartic residues to produce two subunits (large and small), which dimerize to form the active enzyme.

This gene was identified by its ability to cleave and activate the inactive precursor of interleukin-1, a cytokine involved in inflammation, septic shock, and wound healing. It has been shown to induce apoptosis and may function in various developmental stages. Studies in mouse suggest a role in the pathogenesis of Huntington’s disease. Alternative splicing results in transcript variants encoding distinct isoforms.

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