COL9A1 antibody (N-Term)
Quick Overview for COL9A1 antibody (N-Term) (ABIN2788309)
Target
See all COL9A1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- N-Term
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Sequence
- GADGLTGPDG SPGSIGSKGQ KGEPGVPGSR GFPGRGIPGP PGPPGTAGLP
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Predicted Reactivity
- Dog: 86%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Mouse: 79%, Rabbit: 86%, Rat: 79%, Zebrafish: 85%
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Characteristics
- This is a rabbit polyclonal antibody against COL9A1. It was validated on Western Blot.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the N-terminal region of Human COL9A1
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
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Comment
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Antigen size: 678 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- COL9A1 (Collagen, Type IX, alpha 1 (COL9A1))
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Alternative Name
- COL9A1
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Background
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This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20 % ) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene.
Alias Symbols: DJ149L1.1.2, EDM6, FLJ40263, MED, STL4
Protein Interaction Partner: COMP, MAG, COL2A1,
Protein Size: 678 -
Molecular Weight
- 62 kDa
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Gene ID
- 1297
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NCBI Accession
- NM_078485, NP_511040
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UniProt
- A6NEQ6
Target
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