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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 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, Western blot에 최적화되어 있습니다. 인간 반응성을 가지며 액상 형태로 제공됩니다. Affinity chromatography로 정제되었으며, 연구용으로만 사용됩니다.

카탈로그번호
PA569682
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오후 08:38
Thermo Fisher Scientific PA569682 COL11A2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific COL11A2 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.2–1.0 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide directed towards the N-terminal region of human COL11A2
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 2% sucrose
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2689365

Product Specific Information

This target displays homology in the following species:

  • Cow: 91%
  • Dog: 100%
  • Human: 100%
  • Mouse: 92%
  • Pig: 91%
  • Rabbit: 92%

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, and 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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