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ELK Biotechnology FBN1 rabbit pAb
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ELK Biotechnology FBN1 rabbit pAb

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FBN1 rabbit pAb는 인간 Fibrillin-1 단백질을 인식하는 다클론 항체로, WB, IHC, IF, ELISA에 사용 가능. 고순도 IgG 형태로 안정적인 신호 검출 제공. 인간, 마우스, 랫트 반응성 확인. -20°C에서 장기 보관 가능.

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pk
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ELK Biotechnology ES5222-100UL FBN1 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES5222-50UL FBN1 rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology FBN1 rabbit pAb

제품명

FBN1 rabbit pAb

기본 정보

항목 내용
Alternative Names FBN1; FBN; Fibrillin-1
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
ELISA: 1/20000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human Fibrillin-1 (AA range: 2811–2860)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
GeneID (Human) 2200
Human Swiss-Prot No P35555
Species Reactivity Human; Mouse; Rat

세포 내 위치

Secreted. Fibrillin-1 and Asprosin chains are still linked together during secretion from cells, but are subsequently separated by furin (PubMed:24982166).

  • Fibrillin-1: Secreted, extracellular space, extracellular matrix
  • Asprosin: Secreted; secreted by white adipose tissue and circulates in the plasma.

배경 정보

This gene encodes a member of the fibrillin family of proteins. The encoded preproprotein is proteolytically processed to generate two proteins including the extracellular matrix component fibrillin-1 and the protein hormone asprosin.
Fibrillin-1 is an extracellular matrix glycoprotein that serves as a structural component of calcium-binding microfibrils, providing force-bearing structural support in elastic and nonelastic connective tissues throughout the body.
Asprosin, secreted by white adipose tissue, regulates glucose homeostasis. Mutations in this gene are associated with Marfan syndrome, MASS phenotype, ectopia lentis syndrome, Weill-Marchesani syndrome, Shprintzen-Goldberg syndrome, and neonatal progeroid syndrome. (RefSeq, Apr 2016)

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