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

  • 中文名稱:
    SGCG兔多克隆抗體
  • 貨號:
    CSB-PA021186GA01HU
  • 規格:
    ¥3,900
  • 其他:

產品詳情

  • 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,Mouse,Rat
  • 免疫原:
    Human SGCG
  • 免疫原種屬:
    Homo sapiens (Human)
  • 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:
    PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA,WB,IHC
  • 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.
  • 數據庫鏈接:

    HGNC: 10809

    OMIM: 253700

    KEGG: hsa:6445

    STRING: 9606.ENSP00000218867

    UniGene: Hs.37167



主站蜘蛛池模板: 国产麻豆9l精品三级站| 夜夜香夜夜摸夜夜添视频| 亚洲综合av一区二区三区| 国产综合久久久久| 丰满爆乳在线播放| 日本高清在线www3344| 亚洲精品一区久久久久| 国产又黄又硬又粗| 亚洲爆乳无码专区www| 女人高潮抽搐潮喷视频开腿| 国产午夜成人免费看片app| 97精品人人a片免费看| 鲁丝片一区二区三区毛片| 国产免费爽爽视频在线观看| 欧美另类人妖| 熟女体下毛毛黑森林| 国产熟女出轨做受的叫床声| 日韩无套内射高潮| 欧美黑人乱大交| 免费的很黄很污的视频| 美女裸奶100%无遮挡免费网站| 欧美黑人xxxx性高清版| 污污内射久久一区二区欧美日韩| 国产乱了真实在线观看| 日本伦奷在线播放| 先锋影音男人av资源| 日本大乳高潮视频在线观看| 久久老子午夜精品无码怎么打| 日韩欧美激情兽交| 无码av一区二区三区无码| 欧美变态暴力牲交videos| 国产成人av乱码免费观看| 国产极品美女到高潮无套| 成 人 免 费 黄 色| 国产乱人伦真实精品视频| 亚洲五月综合缴情在线| 亚洲mv国产mv在线mv综合试看| 国产精品无码av不卡顿| 色国产精品一区在线观看| 精品亚洲一区二区三区在线播放 | 亚洲一区av无码专区在线观看|