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ELK Biotechnology ABCD1 rabbit pAb
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ELK Biotechnology ABCD1 rabbit pAb

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ABCD1 단백질을 인식하는 토끼 폴리클로날 항체로, WB 및 ELISA에 사용 가능. 인간 ABCD1 유래 펩타이드로 면역화됨. 퍼옥시좀 막 단백질 연구에 적합하며, -20°C에서 1년 보관 가능.

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pk
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ELK Biotechnology ES5186-100UL ABCD1 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES5186-50UL ABCD1 rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology ABCD1 rabbit pAb

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ABCD1 rabbit pAb

제품 정보

항목 내용
Alternative Names ABCD1; ALD; ATP-binding cassette sub-family D member 1; Adrenoleukodystrophy protein; ALDP
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/40000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human ABCD1 (AA range: 531–580)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 75 kD
Gene ID (Human) 215
Human Swiss-Prot No. P33897
Cellular Localization Peroxisome membrane; Multi-pass membrane protein. Mitochondrion membrane; Multi-pass membrane protein. Lysosome membrane; Multi-pass membrane protein. Endoplasmic reticulum membrane; Multi-pass membrane protein.
Species Reactivity Human; Rat; Mouse

Background

The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White).
This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters that require a partner half transporter molecule to form a functional homo- or heterodimeric transporter.
This peroxisomal membrane protein is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder.

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