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          • Primary Antibodies ›
          • COL11A2 Antibodies

          Invitrogen

          COL11A2 Polyclonal Antibody

          View all (9) COL11A2 antibodies

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          Cite COL11A2 Polyclonal Antibody

          COL11A2 Polyclonal Antibody

          Product Details

          PA5-69682

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          0.2-1.0 µg/mL
          -
          Product Specifications

          Species Reactivity

          Human

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          synthetic peptide directed towards the N terminal region of human COL11A2
          View immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          0.5 mg/mL

          Purification

          Affinity chromatography

          Storage buffer

          PBS with 2% sucrose

          Contains

          0.09% sodium azide

          Storage conditions

          -20°C, Avoid Freeze/Thaw Cycles

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          RRID

          AB_2689365

          Product Specific Information

          This target displays homology in the following species: Cow: 91%; Dog: 100%; Human: 100%; Mouse: 92%; Pig: 91%; Rabbit: 92%

          Target Information

          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.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: Collagen alpha-2(XI) chain; collagen, type XI, alpha 2; DAQB-79P13.8; HGNC:2187; pro-a2 chain of collagen type XI

          View more View less

          Gene Aliases: COL11A2; DFNA13; DFNB53; FBCG2; HKE5; PARP; STL3

          View more View less

          UniProt ID: (Human) P13942

          View more View less

          Entrez Gene ID: (Human) 1302

          View more View less

          Function(s)
          protein binding extracellular matrix structural constituent conferring tensile strength protein binding, bridging metal ion binding extracellular matrix structural protein
          Process(es)
          skeletal system development sensory perception of sound collagen fibril organization collagen catabolic process cartilage development palate development soft palate development
          It has to be done as per old AB suggested Products section.
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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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