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Thermo Fisher Scientific COL6A3 Polyclonal Antibody
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Thermo Fisher Scientific COL6A3 Polyclonal Antibody

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COL6A3 단백질을 검출하는 Thermo Fisher Scientific의 폴리클로날 항체. 사람 및 생쥐 시료에 반응하며 IHC(P)와 ICC/IF에 사용 가능. 항원 친화 크로마토그래피로 정제된 액상 형태로, 안정적인 저장 및 높은 특이성을 제공.

카탈로그번호
PA549914
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 05:45
Thermo Fisher Scientific PA549914 COL6A3 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific COL6A3 Polyclonal Antibody

Applications

Immunohistochemistry (Paraffin) (IHC (P))

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 1:100–1:500

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Published Species Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthesized peptide derived from internal of human Collagen VI alpha3 (COL6A3, UniProt ID: P12111-1, antigen range: 2261–2310, antigen length: 3177)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.4, with 50% glycerol, 0.5% BSA
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2635367

Product Specific Information

The antibody detects endogenous levels of total COL6A3 protein.


Target Information

This gene encodes the alpha-3 chain, one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues.
The alpha-3 chain of type VI collagen is much larger than the alpha-1 and -2 chains due to an increased number of subdomains, similar to von Willebrand Factor type A domains, found in the amino terminal globular domain of all alpha chains.
These domains bind extracellular matrix proteins, explaining the importance of this collagen in organizing matrix components.

Mutations in type VI collagen genes are associated with Bethlem myopathy, a rare autosomal dominant proximal myopathy with early childhood onset.
Mutations in this gene also cause Ullrich congenital muscular dystrophy, an autosomal recessive congenital myopathy more severe than Bethlem myopathy.
Multiple transcript variants have been identified, though only some full-length variants are known.
(Information provided by RefSeq, Jun 2009.)


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.


제품 이미지

PA5-49914_COL6A3_P12111-1_Rabbit.svg
PA5-49914_COL6A3_P12111-1_Rabbit_PDP.jpeg

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