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

SGCG Antibody, HRP conjugated

  • 中文名稱:
    SGCG兔多克隆抗體, HRP偶聯(lián)
  • 貨號:
    CSB-PA618771LB01HU
  • 規(guī)格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) SGCG Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    SGCG
  • 別名:
    35 kDa dystrophin associated glycoprotein antibody; 35 kDa dystrophin-associated glycoprotein antibody; 35DAG antibody; 35kD dystrophin associated glycoprotein antibody; 35kDa dystrophin-associated glycoprotein antibody; A4 antibody; DAGA4 antibody; DMDA antibody; DMDA1 antibody; Gamma SG antibody; Gamma-sarcoglycan antibody; Gamma-SG antibody; LGMD2C antibody; MAM antibody; MGC130048 antibody; Sarcoglycan gamma antibody; SCARMD2 antibody; SCG3 antibody; SGCG antibody; SGCG_HUMAN antibody; TYPE antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human Gamma-sarcoglycan protein (108-221AA)
  • 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:
    >95%, Protein G 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:
    Component of the sarcoglycan complex, a subcomplex of the dystrophin-glycoprotein complex which forms a link between the F-actin cytoskeleton and the extracellular matrix.
  • 基因功能參考文獻:
    1. This study showed that fifteen families were shown to carry SGCG variants in patient with early onset severe muscular dystrophy. PMID: 27759885
    2. FADH2-dependent monooxygenase (SgcE6 and SgcC) that catalyzes the hydroxylation of a PCP-tethered substrate PMID: 27560143
    3. These results position archvillin as a mechanically sensitive component of the dystrophin complex and demonstrate that signaling defects caused by loss of gamma-SG occur both at the sarcolemma and in the nucleus. PMID: 25605665
    4. A report of two siblings with severe childhood onset limb-girdle muscular dystrophy type 2C supports the theory that the mutation G787A in the SGCG gene is a founder mutation. PMID: 24534832
    5. Molecular epidemiologic methods were used to calculate the frequency of heterozygotes for this SGCG mutation in Moroccan newborns and to estimate the prevalence of LGMD2C in the Moroccan population. PMID: 24552312
    6. Data suggest that an SNP in an intron of SGCG (rs9552911) is associated with type 2 diabetes [Genome-Wide Association Study in Sikh populations in India & Meta-Analysis] PMID: 23300278
    7. The C allele of the c.-94C>G polymorphism in delta-sarcoglycan is a risk factor for HCM, which is increased by the Amerindian component and can play an important role in the etiology and progression of disease in Mexican patients PMID: 22524166
    8. four Greek Gypsy patients with limb girdle muscular dystrophy type 2C carried the same homozygous C283Y mutation in the gamma-sarcoglycan gene PMID: 20345928
    9. The relative incidence of LGMD2C among Japanese Duchenne muscular dystrophy-like patients can be calculated as 1 in 161 patients suspected to have Duchenne muscular dystrophy. PMID: 20350330
    10. Clinical, histologic, and immunohistochemical characteristics of three children with limb-girdle muscular dystrophy type 2C. Two novel mutations in the gamma-sarcoglycan gene were present. We found phenotypic differences in two brothers. PMID: 15087111
    11. two unrelated patients of Puerto Rican descent who have identical previously undescribed homozygous E263K (G787A) missense mutations on exon 8, and a white North American child with del521T on one allele and a deletion of exon 6 on the other allele. PMID: 16832103
    12. The limb-girdle muscular dystrophy patients with gamma-sarcoglycan deficient LGMD2C do not enable an accurate prediction of the genotype. PMID: 18996010
    13. This study, the first mutational analysis of Indian patients with sarcoglycanopathies suggests gamma SG mutations were the most common and the most prevalent mutation in the gamma SG gene was 525del.T. PMID: 19770540

    顯示更多

    收起更多

  • 相關疾病:
    Limb-girdle muscular dystrophy 2C (LGMD2C)
  • 亞細胞定位:
    Cell membrane, sarcolemma; Single-pass type II membrane protein. Cytoplasm, cytoskeleton.
  • 蛋白家族:
    Sarcoglycan beta/delta/gamma/zeta family
  • 組織特異性:
    Expressed in skeletal and heart muscle.
  • 數(shù)據(jù)庫鏈接:

    HGNC: 10809

    OMIM: 253700

    KEGG: hsa:6445

    STRING: 9606.ENSP00000218867

    UniGene: Hs.37167



主站蜘蛛池模板: 国产精品久久久久影院亚瑟| 欧牲交a欧美牲交aⅴ| 国产极品精品自在线| 亚洲国产欧美在线人成大黄瓜 | 国产精品爱久久久久久久| 精品国产麻豆免费人成网站| 色妺妺免费影院| 久久人妻国产精品31| 2020久热爱精品视频在线观看| 成人av无码一区二区三区| 久久综合狠狠色综合伊人| 人妻少妇乱子伦无码专区| 三级理论中文字幕在线播放| 国产午夜人做人免费视频网站| 国产成人精品av| 亚洲精品无码不卡| 亚洲中文字幕精品久久| 午夜男女爽爽影院免费视频| 伊人久久综合无码成人网| 西西4444www大胆无码| 内射干少妇亚洲69xxx| 一区三区不卡高清影视| 午夜福利不卡片在线机免费视频 | 国产又色又爽又刺激视频| 黑人巨大无码中文字幕无码| 99精品国产福利一区二区| 欧美另类人妖| 亚洲国产精品无码久久98| 久久99精品久久久久久齐齐| 亚洲综合无码av一区二区三区 | 伦理片无码电影在线看| 女人被爽到呻吟gif动态图视看| 国产午国产午夜精华 免费| 国产voyeur精品偷窥222| 精品多人p群无码| 日本少妇毛茸茸高潮| 亚洲人成亚洲精品| 欧美激情精品成人一区| 国产精品99久久久久久宅男小说| 国产乱码一区二区三区| 大肉大捧一进一出好爽mba|