COL11A2 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA577919-Each-of-1 | In Stock | ₹ 48,905.50 |
PIPA577919 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 48,905.50
GST (18%): ₹ 8,802.99
Total Price: ₹ 57,708.49
Antigen
COL11A2
Classification
Polyclonal
Conjugate
Unconjugated
Gene
COL11A2
Gene Alias
COL11A2; Collagen alpha-2(XI) chain; collagen type XI alpha 2; collagen type XI alpha 2 chain; collagen XI-like; collagen, type XI, alpha 2; DAQB-79P13.8; DFNA13; DFNB53; FBCG2; HGNC:2187; HKE5; PARP; pro-a2 chain of collagen type XI; procollagen, type XI, alpha 2; putative collagen XI; STL3; type XI collagen alpha2 chain
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
1302
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Western Blot
Concentration
0.76 mg/mL
Formulation
PBS with 20% glycerol and 0.01% thimerosal; pH 7
Gene Accession No.
P13942
Gene Symbols
COL11A2
Immunogen
Recombinant protein encompassing a sequence within the N-terminus region of human COL11A2. The exact sequence is proprietary.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Positive Control: human COLC11A2-transfected 293T cells (partial fragment) Predicted Reactivity: Mouse (89%), Rat (89%), Bovine (93%) Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- 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), and 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.