在线日韩日本国产亚洲丨少妇伦子伦情品无吗丨欧美性猛交xxxx免费看蜜桃丨精品人妻系列无码一区二区三区丨亚洲精品无码不卡在线播放

Your Good Partner in Biology Research

COL9A2 Antibody, HRP conjugated

  • 中文名稱:
    COL9A2兔多克隆抗體, HRP偶聯
  • 貨號:
    CSB-PA617900OB01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) COL9A2 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
  • 別名:
    CO9A2_HUMAN antibody; COL9A2 antibody; Collagen alpha-2(IX) chain antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Peptide sequence from Human Collagen alpha-2(IX) chain protein (594-611AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    HRP
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    Antigen Affinity Purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA
  • Protocols:
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 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.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能:
    Structural component of hyaline cartilage and vitreous of the eye.
  • 基因功能參考文獻:
    1. rs12077871, rs12722877, and rs7533552 variants in COL9A2 were not significantly associated with a predisposition to lumbar disc degeneration. PMID: 29506578
    2. Study provides evidence that the COL9A2 Gln326Arg polymorphism contributes to the development of intervertebral disc disease in the Chinese population. PMID: 28002589
    3. Meta-analysis. Our results suggest that the COL9A2 rs12077871, rs12722877, and rs7533552 polymorphisms may not be associated with lumbar disc disease. PMID: 24983932
    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. PMID: 24711017
    5. The allelic variants in the collagen IX genes - COL9A2 and COL9A3 have been identified as genetic risk factors for intervertebral disc disease--{review} PMID: 24636772
    6. Studies indicate that two SNPs that introduce tryptophan polymorphisms in COL9A2 and COL9A3 are independently linked to an increased risk of lumbar disc disease. PMID: 21311409
    7. 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. PMID: 21228751
    8. loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome PMID: 21671392
    9. 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. PMID: 21159828
    10. 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 PMID: 12244547
    11. 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. PMID: 12782139
    12. The collagen IX is cartilage specific, and expressed in hypertrophic chondrocytes and bone. PMID: 15625128
    13. 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. PMID: 16371896
    14. 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. PMID: 16440132
    15. Association of a COL9A2 specific haplotype with lumbar disc disease in the Japanese population. PMID: 17024315
    16. 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. PMID: 18080148
    17. COL9A2 polymorphisms were associated with intervertebral disc mechanics, relating genetic variations and debilitating mechanical alterations that may ultimately result in intervertebral disc degeneration. PMID: 18246003

    顯示更多

    收起更多

  • 相關疾病:
    Multiple epiphyseal dysplasia 2 (EDM2); Intervertebral disc disease (IDD); Stickler syndrome 5 (STL5)
  • 亞細胞定位:
    Secreted, extracellular space, extracellular matrix.
  • 蛋白家族:
    Fibril-associated collagens with interrupted helices (FACIT) family
  • 數據庫鏈接:

    HGNC: 2218

    OMIM: 120260

    KEGG: hsa:1298

    STRING: 9606.ENSP00000361834

    UniGene: Hs.418012



主站蜘蛛池模板: 午夜精品一区二区三区在线观看| 欧美xxxx做受欧美1314| 久久国产精品99久久久久久口爆| 97色成人综合网站| 在线观看成人无码中文av天堂不卡| 人妻少妇精品久久| 奇米影视第四色首页| 国产亚洲欧美日韩夜色凹凸成人| 免费va国产高清大片在线| 国产在线高清视频无码| 成人性做爰aaa片免费看曹查理| 少妇太爽了在线观看免费视频| 亚洲国产精品18久久久久久| 久久久久久久岛国免费观看 | 久久这里只精品国产免费9| 东京热加勒比视频一区| 欧美在线精彩视频免费播放 | 国产精品性夜天天拍拍2021| 国产午睡沙发被弄醒完整版| 宝宝好涨水快流出来免费视频| 少妇被猛男粗大的猛进出| 国产蝌蚪视频一区二区三区| 国产精品a久久777777| 四虎成人精品一区二区免费网站| 亚 洲 视 频 高 清 无 码 | 久久青青草原国产免费播放| 日韩经典精品无码一区| 中文字幕欧美亚州视频免费| 免费裸体美女网站| 精品人妻中文字幕有码在线| 免费看撕开奶罩揉吮奶头视频| 蜜臀av999无码精品国产专区 | 欧美一区二区三区视频在线观看 | 少妇无码av无码专线区大牛影院| 国产精品久久| 中文字幕亚洲日韩无线码| 人妻熟女 视频二区 视频一区| 大香伊蕉日本一区二区| 人妻体验按摩到忍不住哀求继续 | 色综合久久精品亚洲国产| 国产福利高颜值在线观看|