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Thermo Fisher Scientific COL11A2 Polyclonal Antibody
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Thermo Fisher Scientific COL11A2 Polyclonal Antibody

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COL11A2 단백질을 인식하는 토끼 폴리클로날 항체로, Western blot 및 IHC(P) 분석에 적합합니다. 인간 및 생쥐 시료에 반응하며, 항원 친화 크로마토그래피로 정제되었습니다. 고순도(>95%) 제품으로 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 03. 오후 10:48
Thermo Fisher Scientific PA577258 COL11A2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific COL11A2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to amino acids 1200–1250 of Human COL11A2
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2720985

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 near the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer, where the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing produces PARP, a proline/arginine-rich protein.
Mutations in this gene are associated with several disorders including:

  • Type III Stickler syndrome
  • Oto-spondylo-megaepiphyseal dysplasia (OSMED syndrome)
  • Weissenbacher-Zweymuller syndrome
  • Autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13)
  • Autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53)

Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6.


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

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