
Thermo Fisher Scientific COL11A2 Polyclonal Antibody
COL11A2 단백질을 인식하는 Rabbit Polyclonal 항체로, Western Blot에 적합합니다. 인간 시료에 반응하며, 마우스·랫·소에서도 예측 반응성을 보입니다. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol 용액 형태로 제공됩니다. 연구용으로만 사용 가능합니다.
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- PA577919
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- pk
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Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:1,000–1:10,000 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein encompassing a sequence within the N-terminus region of human COL11A2 (exact sequence proprietary) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.76 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7, with 20% glycerol |
| Contains | 0.01% thimerosal |
| 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_2735673 |
Product Specific Information
- Positive Control: Human COL11A2-transfected 293T cells (partial fragment)
- Predicted Reactivity: Mouse (89%), Rat (89%), Bovine (93%)
- Note: 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.
⚠ WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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