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

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