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Thermo Fisher Scientific COL11A2 Monoclonal Antibody (GT6410)
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Thermo Fisher Scientific COL11A2 Monoclonal Antibody (GT6410)

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COL11A2 단백질을 인식하는 Mouse monoclonal antibody (GT6410). Western blot에 적합하며 Human, Mouse, Rat에 반응. Protein G로 정제된 액상 형태로 제공되며, 4°C 단기 보관 및 -20°C 장기 보관 권장. 연구용으로만 사용 가능.

카탈로그번호
MA531484
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 08:31
Thermo Fisher Scientific MA531484 COL11A2 Monoclonal Antibody (GT6410) 100 ul pk판매 단위 pk ·
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657,900원VAT 포함 723,690원

Thermo Fisher Scientific · Thermo Fisher Scientific COL11A2 Monoclonal Antibody (GT6410)

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:3,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone GT6410
Immunogen Recombinant protein encompassing a sequence within the N-terminus region of human COL11A2
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains No preservative
Storage Conditions Store at 4°C short term; for long term, store at -20°C avoiding freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2787115

Product Specific Information

  • Keep as concentrated solution.
  • Predicted reactivity: Mouse (85%), Rat (85%), Bovine (93%).
  • Positive Control: human COL11A2-transfected 293T (N-terminal fragment of COL11A2 isoform 1).
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

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 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer, but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain.

Mutations in this gene are associated with:

  • Type III Stickler syndrome
  • Otospondylomegaepiphyseal 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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