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Last updated: 2016/12/4
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COL11A2 polyclonal antibody

  • Catalog # : PAB6952
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of COL11A2.
  • Immunogen:
  • A synthetic peptide corresponding to human COL11A2.
  • Sequence:
  • QKELECEGGQRERPQ
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 172, 162, 160
  • Specificity:
  • This antibody is expected to recognize all three reported isoforms (NP_542411.1, NP_542412.1, NP_542410.1).
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:1000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Publication Reference
  • Applications
  • ELISA
  • Application Image
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 1302
  • Protein Accession#:
  • NP_542411.1;NP_542412.1;NP_542410.1
  • Gene Name:
  • COL11A2
  • Gene Alias:
  • DFNA13,DFNB53,HKE5,PARP,STL3
  • Gene Description:
  • collagen, type XI, alpha 2
  • Gene Summary:
  • 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
  • Other Designations:
  • OTTHUMP00000029040,collagen alpha-2(XI) chain,collagen alpha2(XI),pro-a2 chain of collagen type XI,pro-a2(XI)
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