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ELK Biotechnology Caspase-8 (phospho Ser347) rabbit pAb
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ELK Biotechnology Caspase-8 (phospho Ser347) rabbit pAb

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Caspase-8의 Ser347 인산화 부위를 인식하는 토끼 폴리클로날 항체로, 세포 사멸 연구에 적합합니다. WB, IHC, IF, ELISA에 사용 가능하며, 사람 및 랫트 시료에 반응합니다. -20°C에서 1년 보관 가능합니다.

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pk
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ELK Biotechnology ES7727-100UL Caspase-8 (phospho Ser347) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7727-50UL Caspase-8 (phospho Ser347) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Caspase-8 (phospho Ser347) rabbit pAb

Caspase-8 (phospho Ser347) rabbit pAb

제품 정보

항목 내용
Product name Caspase-8 (phospho Ser347) rabbit pAb
Alternative Names CASP8; MCH5; Caspase-8; CASP-8; Apoptotic cysteine protease; Apoptotic protease Mch-5; CAP4; FADD-homologous ICE/ced-3-like protease; FADD-like ICE; FLICE; ICE-like apoptotic protease 5; MORT1-associated ced-3 homolog; MACH
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500–1/2000
Immunohistochemistry: 1/100–1/300
ELISA: 1/5000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human Caspase 8 around the phosphorylation site of Ser347 (AA range: 313–362)
Storage -20°C / 1 year
Host Rabbit
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 55 kD
Gene ID (Human) 841
Human Swiss-Prot No. Q14790
Cellular Localization Cytoplasm, Nucleus
Species Reactivity Human, Rat

Background

This gene encodes 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 composed of a prodomain, a large protease subunit, and a small protease subunit. Activation requires proteolytic processing at conserved internal aspartic residues to generate a heterodimeric enzyme consisting of the large and small subunits. This protein is involved in programmed cell death induced by Fas and various apoptotic stimuli. The N-terminal FADD-like death effector domain suggests interaction with Fas-interacting protein FADD. It was detected in insoluble fractions of affected brain regions from Huntington disease patients, implicating a potential role in neurodegenerative diseases.

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