
Thermo Fisher Scientific COL11A2 Monoclonal Antibody (GT6410)
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.
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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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