COL11A2 rabbit pAb

CAT:
855-ES2019-01
Size:
50 µL
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
COL11A2 rabbit pAb - image 1

COL11A2 rabbit pAb

  • Background:

    Collagen type XI alpha 2 chain (COL11A2) Homo sapiens 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. [provided by RefSeq, Jul 2009]
  • Description:

    Collagen type XI alpha 2 chain (COL11A2) Homo sapiens 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. [provided by RefSeq, Jul 2009],
  • UniProt:

    P13942
  • Swiss Prot:

    P13942
  • Reactivity:

    Human; Mouse
  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human Collagen XI alpha2. AA range:1211-1260
  • Clonality:

    Polyclonal
  • Source:

    Rabbit
  • Applications:

    WB; IHC; IF; ELISA
  • Concentration:

    1 mg/ml
  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.
  • Molecular Weight:

    171kD
  • Storage Conditions:

    -20°C/1 year
  • Observed Molecular Weight:

    171kD
  • Fragment:

    IgG
  • Subcellular Location:

    Secreted, extracellular space, extracellular matrix .
  • Other Product Names:

    COL11A2; Collagen alpha-2 (XI) chain
  • Gene ID (Human):

    1302