COL9A3 Antibody
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中文名稱：COL9A3兔多克隆抗體
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貨號：CSB-PA833813
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規格：￥2024
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圖片：
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Immunohistochemistry analysis of paraffin-embedded human tonsil tissue using Collagen IX α3 antibody. -
Immunofluorescence analysis of NIH/3T3 cells, using Collagen IX α3 antibody.
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) COL9A3 Polyclonal antibody
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Uniprot No.：
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基因名：
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宿主：Rabbit
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反應種屬：Human
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免疫原：Synthesized peptide derived from internal of Human Collagen IX α3.
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免疫原種屬：Homo sapiens (Human)
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克隆類型：Polyclonal
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純化方式：The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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濃度：It differs from different batches. Please contact us to confirm it.
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產品提供形式：Liquid
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應用范圍：ELISA,IHC,IF
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推薦稀釋比：
Application Recommended Dilution IHC 1:50-1:100 IF 1:100-1:500 -
Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期：Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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功能：Structural component of hyaline cartilage and vitreous of the eye.
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基因功能參考文獻：
- rs61734651 variant in COL9A3 was not significantly associated with a predisposition to lumbar disc degeneration. PMID: 29506578
- In an Iranian population, we observed a 5.8-fold increase in the odds of degenerative disc disease in males when the Trp3 allele was present PMID: 27798555
- A novel missense mutation was identified in a family diagnosed with multiple epiphyseal dysplasia. PMID: 25381065
- Here, we describe the first autosomal recessive Stickler family due to loss of function mutations (c.1176_1198del, p.Gln393Cysfs*25) of COL9A3 gene. These findings extend further the role of collagen genes family in the disease pathogenesis. PMID: 24273071
- We report an 81% mutation detection rate for pseudoachondroplasia, of which COMP+Col9A3 mutations were more prevalent (61%) than COMP mutations alone (30%). PMID: 21042783
- Patients with COL9A3 in-frame deletion of three amino acid residues (G181-P183 del) and missense mutation (D617E) showed moderate progressive bilateral sensorineural hearing impairment in all frequencies. PMID: 15917166
- a fragment of collagen type IX alpha chain is found in 34% of newborns with ureteropelvic junction obstruction, and in 100% of normals. PMID: 17701042
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相關疾病：Multiple epiphyseal dysplasia 3 (EDM3); Intervertebral disc disease (IDD)
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亞細胞定位：Secreted, extracellular space, extracellular matrix.
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蛋白家族：Fibril-associated collagens with interrupted helices (FACIT) family
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數據庫鏈接：
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