Collagen Type IX alpha 2 (COL9a2) ELISA Kits

COL9a2 encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Additionally we are shipping Collagen Type IX alpha 2 Antibodies (5) and and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
COL9a2 1298 Q14055
COL9a2 12840  
Anti-Rat COL9a2 COL9a2 362584  
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Top Collagen Type IX alpha 2 ELISA Kits at antibodies-online.com

Showing 3 out of 7 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 0.078 ng/mL 0.312-20 ng/mL   96 Tests Log in to see 15 to 18 Days
$910.56
Details
Mouse 19.53 pg/mL n/a   96 Tests Log in to see 15 to 18 Days
$910.56
Details
Chicken
  96 Tests Log in to see 15 to 18 Days
$1,095.60
Details

More ELISA Kits for Collagen Type IX alpha 2 Interaction Partners

Human Collagen Type IX alpha 2 (COL9a2) interaction partners

  1. rs12077871, rs12722877, and rs7533552 variants in COL9A2 were not significantly associated with a predisposition to lumbar disc degeneration.

  2. Study provides evidence that the COL9A2 Gln326Arg polymorphism contributes to the development of intervertebral disc disease in the Chinese population.

  3. Meta-analysis. Our results suggest that the COL9A2 rs12077871, rs12722877, and rs7533552 polymorphisms may not be associated with lumbar disc disease.

  4. Two novel mutations, c.143G>C in exon 2 and c.884G>A in exon 17 of the COL9A2 gene, may contribute to the development of pathological myopia.

  5. The allelic variants in the collagen IX genes - COL9A2 and COL9A3 have been identified as genetic risk factors for intervertebral disc disease--{review}

  6. The NC2 domain of type IX collagen determines the chain composition but also the chain register of the triple helix.

  7. Studies indicate that two SNPs that introduce tryptophan polymorphisms in COL9A2 and COL9A3 are independently linked to an increased risk of lumbar disc disease.

  8. Data indicate that no causal SNPs in COL9A2 were significantly associated with LSS, but Haplotype Analysis showed that the "GCAGCG" haplotype (HAP2) was overrepresented in LSS patients.

  9. loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome

  10. Data show that the associating G allele in COL9A2 changes a glutamine to arginine or to tryptophan and may predispose to both hip osteoarthritis and lumbar disc degeneration, making it a candidate for degenerative connective tissue diseases.

  11. This study extends the range of gene-mutations that can cause multiple epiphyseal dysplasia-related myopathy.

  12. mutations leading to skipping of exon 3 within the COL3 domain of the alpha2-chain of collagen type IX may be relatively common in patients with a special subtype of multiple epiphyseal dysplasia

  13. Both Trp2 and Trp3 allelic products are incorporated into cross-linked fibrillar network of developing human cartilage apparently normally. Any pathological consequences are likely to be long-term and indirect rather than from overt misassembly of matrix.

  14. The collagen IX is cartilage specific, and expressed in hypertrophic chondrocytes and bone.

  15. A population study using magnetic resonance imaging to define degenerative disc disease demonstrates that the TRP2 allele (Gln326Trp)of COL9A2 is a significant risk factor for development and severity of degeneration.

  16. A Japanese family with an autosomal dominant multiple epiphyseal dysplasia (MED EDM2) was studied; genomic analysis for COL9A2 identified an Ex3-1A>G heterozygous mutation, which has been proved to result in skipping of exon 3.

  17. Association of a COL9A2 specific haplotype with lumbar disc disease in the Japanese population.

  18. Homozygosity for the Arg allele of Col9A2 seems to be more frequent in the patient group with early recurrence although the differences in the allele frequencies were statistically not significant.

  19. COL9A2 polymorphisms were associated with intervertebral disc mechanics, relating genetic variations and debilitating mechanical alterations that may ultimately result in intervertebral disc degeneration.

Mouse (Murine) Collagen Type IX alpha 2 (COL9a2) interaction partners

  1. Results show that absence of Col IX induces early developmental, structural and biomechanical alterations in both vertebral body and intervertebral disc which eventually cause severe degenerative changes in the aging spine.

Collagen Type IX alpha 2 (COL9a2) Antigen Profile

Antigen Summary

This gene encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Type IX collagen, a heterotrimeric molecule, is usually found in tissues containing type II collagen, a fibrillar collagen. This chain is unusual in that, unlike the other two type IX alpha chains, it contains a covalently attached glycosaminoglycan side chain. Mutations in this gene are associated with multiple epiphyseal dysplasia.

Gene names and symbols associated with COL9a2

  • collagen type IX alpha 2 chain (COL9A2) antibody
  • collagen, type IX, alpha 2 (Col9a2) antibody
  • collagen type IX alpha 2 chain (Col9a2) antibody
  • AI427499 antibody
  • Col9a-2 antibody
  • DJ39G22.4 antibody
  • EDM2 antibody
  • MED antibody
  • STL5 antibody

Protein level used designations for COL9a2

alpha 2 type IX collagen , collagen IX, alpha-2 polypeptide , collagen alpha-2(IX) chain , procollagen, type IX, alpha 2 , alpha 1 type IX collagen

GENE ID SPECIES
1298 Homo sapiens
12840 Mus musculus
362584 Rattus norvegicus
396524 Gallus gallus
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