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ELK Biotechnology Laminin α-3 rabbit pAb
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ELK Biotechnology Laminin α-3 rabbit pAb

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Laminin α-3 단백질을 인식하는 토끼 다클론 항체로, WB, IHC, IF, ELISA에 사용 가능. 인간, 마우스, 랫트 반응성. 합성 펩타이드(AA 2571-2620)로 면역화. 세포외기질 및 기저막 단백질 연구에 적합.

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pk
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ELK Biotechnology ES6075-100UL Laminin α-3 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES6075-50UL Laminin α-3 rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Laminin α-3 rabbit pAb

ELK Biotechnology Laminin α-3 rabbit pAb

제품 정보

항목 내용
Product name Laminin α-3 rabbit pAb
Alternative Names LAMA3; LAMNA; Laminin subunit alpha-3; Epiligrin 170 kDa subunit; E170; Epiligrin subunit alpha; Kalinin subunit alpha; Laminin-5 subunit alpha; Laminin-6 subunit alpha; Laminin-7 subunit alpha; Nicein subunit alpha
Applications WB; IHC; IF; ELISA
Recommended Dilutions WB: 1/500–1/2000; IHC: 1/100–1/300; IF: 1/200–1/1000; ELISA: 1/40000; Not yet tested in other applications
Immunogen Synthesized peptide derived from human LAMA3 (AA range: 2571–2620)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 120, 60 kDa
Gene ID (Human) 3909
Human Swiss-Prot No. Q16787
Cellular Localization Secreted, extracellular space, extracellular matrix, basement membrane (major component)
Species Reactivity Human; Mouse; Rat

Background

The protein encoded by this gene belongs to the laminin family of secreted molecules. Laminins are heterotrimeric molecules composed of alpha, beta, and gamma subunits that assemble through a coiled-coil domain. They are essential for the formation and function of the basement membrane and play roles in regulating cell migration and mechanical signal transduction. This gene encodes an alpha subunit responsive to several epithelial-mesenchymal regulators, including keratinocyte growth factor, epidermal growth factor, and insulin-like growth factor. Mutations in this gene are associated with Herlitz type junctional epidermolysis bullosa and laryngoonychocutaneous syndrome. Alternative splicing and promoter usage result in multiple transcript variants. (RefSeq, Dec 2014)

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