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ELK Biotechnology Cleaved-Caspase-1 p20 (D210) rabbit pAb
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ELK Biotechnology Cleaved-Caspase-1 p20 (D210) rabbit pAb

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Cleaved-Caspase-1 p20 (D210) rabbit polyclonal antibody. 인간, 마우스, 랫트 시료에 반응하며 WB, IF, IHC, ELISA에 사용 가능. Caspase-1 활성화 단백질 검출용. 세포자멸사 연구 및 염증 반응 분석에 적합.

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pk
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ELK Biotechnology ES7675-100UL Cleaved-Caspase-1 p20 (D210) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7675-50UL Cleaved-Caspase-1 p20 (D210) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Cleaved-Caspase-1 p20 (D210) rabbit pAb

Cleaved-Caspase-1 p20 (D210) rabbit pAb

제품 개요

Cleaved-Caspase-1 p20 (D210) rabbit polyclonal antibody는 Caspase-1 단백질의 절단형(p20 fragment)을 인식하는 항체로, 세포자멸사(apoptosis) 및 염증 관련 연구에 활용됩니다.

제품 정보

항목 내용
Product Name Cleaved-Caspase-1 p20 (D210) 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; IF; IHC; ELISA
Recommended Dilutions WB 1:500–2000, IHC-p 1:50–300, IF 1:50–300
Immunogen Synthesized peptide derived from human Caspase-1 (AA range: 161–210)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 25 kDa
Gene ID (Human) 834
Human Swiss-Prot No. P29466
Cellular Localization Cytoplasm, Cell membrane
Species Reactivity Human, Mouse, Rat

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) that dimerize to form the active enzyme.
Caspase-1 is known for 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 models suggest a role in the pathogenesis of Huntington’s disease.
Alternative splicing results in transcript variants encoding distinct isoforms. (RefSeq, Mar 2012)

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