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Browse our anti-COL11A2 (COL11A2) Antibodies

Full name:
anti-Collagen, Type XI, alpha 2 Antibodies (COL11A2)
On are 31 Collagen, Type XI, alpha 2 (COL11A2) Antibodies from 6 different suppliers available. Additionally we are shipping COL11A2 Kits (11) and and many more products for this protein. A total of 46 COL11A2 products are currently listed.
list all antibodies Gene Name GeneID UniProt
COL11A2 1302 P13942
COL11A2 12815 Q64739
Anti-Rat COL11A2 COL11A2 294279  

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anti-Human COL11A2 Antibodies:

anti-Mouse (Murine) COL11A2 Antibodies:

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Top referenced anti-COL11A2 Antibodies

  1. Human Polyclonal COL11A2 Primary Antibody for WB - ABIN2784122 : Karppinen, Daavittila, Solovieva, Kuisma, Taimela, Natri, Haapea, Korpelainen, Niinimäki, Tervonen, Ala-Kokko, Männikkö: Genetic factors are associated with modic changes in endplates of lumbar vertebral bodies. in Spine 2008 (PubMed)

  2. Human Polyclonal COL11A2 Primary Antibody for ELISA, WB - ABIN560431 : Mercuri, Gill, Simionescu: Novel tissue-derived biomimetic scaffold for regenerating the human nucleus pulposus. in Journal of biomedical materials research. Part A 2010 (PubMed)

  3. Human Polyclonal COL11A2 Primary Antibody for ELISA, WB - ABIN185560 : Harel, Rabinowitz, Hendler, Galil, Flusser, Chemke, Gradstein, Lifshitz, Ofir, Elbedour, Birk: COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED). in American journal of medical genetics. Part A 2004 (PubMed)

More Antibodies against COL11A2 Interaction Partners

Human Collagen, Type XI, alpha 2 (COL11A2) interaction partners

  1. Data indicate that Ala37Ser is the missense mutation located in the NC4 domain of the collagen type XI (show COL11A1 Antibodies) COL11A2 protein.

  2. Expanded spectrum of mutations in the COL11A1 (show COL11A1 Antibodies) and COL11A2 genes in Stickler syndrome.

  3. A novel mutation in COL11A2 was found in a Japanese family with non-ocular Stickler syndrome.

  4. Hearing impairment in non-ocular Stickler syndrome is characterized by non-progressive hearing loss, present since childhood, and mostly mild to moderate in severity. Heterozygote mutations in COL11A2 were present in two pedigrees.

  5. These findings thus demonstrate that fibrochondrogenesis can result from either recessively or dominantly inherited mutations in COL11A2

  6. The findings of a significant association between lip and/or palate clefts and two markers in the WNT3 (show WNT3 Antibodies) and COL11A2 genes were the most consistent and were observed in all groups analysed and stratified.

  7. four loci showed the strongest associations with RA (P<0.005): ZNF391 (show ZNF391 Antibodies), OR2H1 (show OR2H1 Antibodies), C6orf26-RDBP (show RDBP Antibodies) and HLA-DPB1 (show HLA-DPB1 Antibodies)-COL11A2.

  8. A novel homozygous COL11A2 deletion causes a C-terminal protein truncation with incomplete mRNA decay in a Turkish patient.

  9. individuals carrying the C allele at the COL11A2 SNP site, rs2076311, had a lower risk of Kawasaki disease and had a lower probability of developing coronary artery lesions

  10. implication of IRF6 (show IRF6 Antibodies), COL2A1 (show COL2A1 Antibodies), and WNT3 (show WNT3 Antibodies) in occurrence of nonsyndromic cleft palate (NSCP); likely variation in cartilage collagen (show COL2A1 Antibodies) II and XI genes, IRF6 (show IRF6 Antibodies), and Wnt (show WNT2 Antibodies) and FGF signal pathway genes contributes susceptibility to NSCP in Northeast Europe populations

Mouse (Murine) Collagen, Type XI, alpha 2 (COL11A2) interaction partners

  1. The expression patterns suggest essential roles for Col11a1 (show COL11A1 Antibodies) and Col11a2 in the basilar or tectorial membranes.

  2. The present study has revealed a novel retinoic acid-response element in Col11a2 that does not interact directly with the promoter, but instead requires the D/E enhancer to mediate transcriptional activation.

COL11A2 Antigen Profile

Antigen 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.

Alternative names and synonyms associated with COL11A2

  • collagen, type XI, alpha 2 (col11a2) antibody
  • collagen, type XI, alpha 2 (COL11A2) antibody
  • bromodomain containing 2 (BRD2) antibody
  • collagen, type XI, alpha 2 (Col11a2) antibody
  • COL11A2 antibody
  • DFNA13 antibody
  • DFNB53 antibody
  • FBCG2 antibody
  • HKE5 antibody
  • MGC89039 antibody
  • PARP antibody
  • RING3 antibody
  • STL3 antibody

Protein level used designations for COL11A2

collagen, type XI, alpha 2 , collagen alpha-2(XI) chain-like , bromodomain-containing protein 2 , collagen type XI alpha 2 , collagen alpha-2(XI) chain , pro-a2 chain of collagen type XI , procollagen, type XI, alpha 2 , type XI collagen alpha2 chain

448277 Xenopus (Silurana) tropicalis
462600 Pan troglodytes
100061226 Equus caballus
100435198 Pongo abelii
100476192 Ailuropoda melanoleuca
100141307 Sus scrofa
1302 Homo sapiens
481734 Canis lupus familiaris
515435 Bos taurus
12815 Mus musculus
294279 Rattus norvegicus
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