产品封面图

肌萎缩相关蛋白DAG1抗体

收藏
  • ¥1900
  • Biorigin
  • BN41046R
  • 2025年08月04日
  • IHC-P,
  • Human,Mouse,Rat,Chicken,Dog,Pig,Horse,Rabbit,
avatar
  • 企业认证

    点击 QQ 联系

    • 详细信息
    • 文献和实验
    • 技术资料
    • 适应物种

      Human,Mouse,Rat,Chicken,Dog,Pig,Horse,Rabbit,

    • 应用范围

      IHC-P,

    • 抗体英文名

      Alpha Dystroglycan

    • 规格

      100ul

    英文名称 Alpha Dystroglycan
    中文名称 肌萎缩相关蛋白DAG1抗体
    别    名 AGRNR; Alpha-DG; Beta-DG; Beta-dystroglycan; beta Dystroglycan; DAG; Dag1; DAG1_HUMAN; Dystroglycan 1 (dystrophin-associated glycoprotein 1); Dystroglycan; Dystrophin-associated glycoprotein 1; 156DAG; A3a; Dystrophin-associated glycoprotein 1.  
    研究领域 免疫学  神经生物学  信号转导  转录调节因子  细胞骨架  细胞外基质  
    抗体来源 Rabbit
    克隆类型 Polyclonal
    交叉反应 Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Horse, Rabbit, )
    产品应用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:200-800 (石蜡切片需做抗原修复)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量 98kDa
    细胞定位 细胞核 细胞浆 细胞膜 细胞外基质 分泌型蛋白 
    性    状 Liquid
    浓    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human DAG1:451-550/895 
    亚    型 IgG
    纯化方法 affinity purified by Protein A
    储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMed PubMed
    产品介绍 Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.[provided by RefSeq, Apr 2010]

    Function:
    The dystroglycan complex is involved in a number of processes including laminin and basement membrane assembly, sarcolemmal stability, cell survival, peripheral nerve myelination, nodal structure, cell migration, and epithelial polarization.
    Alpha-dystroglycan is an extracellular peripheral glycoprotein that acts as a receptor for both extracellular matrix proteins containing laminin-G domains, and for certain adenoviruses. Receptor for laminin-2 (LAMA2) and agrin in peripheral nerve Schwann cells. Also acts as a receptor for M.leprae in peripheral nerve Schwann cells but only in the presence of the G-domain of LAMA2, and for lymphocytic choriomeningitis virus, Old World Lassa fever virus, and clade C New World arenaviruses.
    Beta-dystroglycan is a transmembrane protein that plays important roles in connecting the extracellular matrix to the cytoskeleton. Acts as a cell adhesion receptor in both muscle and non-muscle tissues. Receptor for both DMD and UTRN and, through these interactions, scaffolds axin to the cytoskeleton. Also functions in cell adhesion-mediated signaling and implicated in cell polarity.

    Subunit:
    Monomer. Heterodimer of alpha- and beta-dystroglycan subunits which are the central components of the dystrophin-glycoprotein complex.

    Subcellular Location:
    Secreted > extracellular space and Cell membrane. Cytoplasm > cytoskeleton. Nucleus > nucleoplasm. The monomeric form translocates to the nucleus via the action of importins and depends on RAN. Nuclear transport is inhibited by Tyr-892 phosphorylation. In skeletal muscle, this phosphorylated form locates to a vesicular internal membrane compartment. In peripheral nerves, localizes to the Schwann cell membrane. Colocalizes with ERM proteins in Schwann-cell microvilli.

    Tissue Specificity:
    Expressed in a variety of fetal and adult tissues. In epidermal tissue, located to the basement membrane. Also expressed in keratinocytes and fibroblasts.

    Post-translational modifications:
    O- and N-glycosylated. Alpha-dystroglycan is heavily O-glycosylated comprising of up to two thirds of its mass and the carbohydrate composition differs depending on tissue type. Mucin-type O-glycosylation is important for ligand binding activity. O-mannosylation of alpha-DAG1 is found in high abundance in both brain and muscle where the most abundant glycan is Sia-alpha-2-3-Gal-beta-1-4-Glc-NAc-beta-1-2-Man. In muscle, glycosylation on Thr-379 by a phosphorylated O-mannosyl glycan with the structure 2-(N-acetylamido)-2-deoxygalactosyl-beta-1,3-2-(N-acetylamido)-2-deoxyglucosyl-beta-1,4-6-phosphomannose is mediated by like-acetylglucosaminyltransferase (LARGE) protein and is required for laminin binding. O-mannosylation is also required for binding lymphocytic choriomeningitis virus, Old World Lassa fever virus, and clade C New World arenaviruses. The O-glycosyl hexose on Thr-367, Thr-369, Thr-372, Thr-381 and Thr-388 is probably mannose. O-glycosylated in the N-terminal region with a core 1 or possibly core 8 glycan. The beta subunit is N-glycosylated. Autolytic cleavage produces the alpha and beta subunits. In cutaneous cells, as well as in certain pathological conditions, shedding of beta-dystroglcan can occur releasing a peptide of about 30 kDa.
    SRC-mediated phosphorylation of the PPXY motif of the beta subunit recruits SH2 domain-containing proteins, but inhibits binding to WWW domain-containing proteins, DMD and UTRN. This phosphorylation also inhibits nuclear entry.

    Similarity:
    Contains 1 peptidase S72 domain.

    SWISS:
    Q14118

    Gene ID:
    1605

    Database links:

    Entrez Gene: 1605 Human

    Entrez Gene: 13138 Mouse

    Entrez Gene: 100009278 Rabbit

    Entrez Gene: 114489 Rat

    Omim: 128239 Human

    SwissProt: Q14118 Human

    SwissProt: Q62165 Mouse

    Unigene: 76111 Human

    Unigene: 7524 Mouse

    Unigene: 36260 Rat



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

     

    风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。

    图标文献和实验
    相关实验
    • 胶体金免疫层析法对抗幽门螺杆菌相关蛋白A抗体的检测

      金酸(HAuCl·Cl3 ·4H2 O) 2. 葡萄球菌A蛋白(SPA) 3. 细胞毒素相关蛋白A(CagA) 4. 酶联免疫吸附试验(ELISA)检测抗CagA-IgG试剂盒 实验设备   1. Z 323 K低温高速离心机 2. LGJ 0.5-Ⅱ冷冻干燥机 3. 点膜器 实验材料   血清标本 实验步骤  

    • 胶体金免疫层析法检测抗幽门螺杆菌细胞毒素相关蛋白A抗体

      摘 要: 目的 建立一种快速、简易的检测血清中抗幽门螺杆菌(Hp)细胞毒素相关蛋白A(CagA)抗体的胶体金免疫层析法(GICA)。 方法 采用柠檬酸三钠还原法制备胶体金颗粒,标记葡萄球菌A蛋白(SPA),将重组的CagA抗原划线固定于硝酸纤维素膜上,制成免疫层析检测试条。 血清中IgG与测试条上金标记物结合后沿着硝酸纤维素膜移动,与膜上的固相抗体结合形成肉眼可见的红色线条。 结果 用GICA与ELISA试剂盒对比检测

    • 近 300 万中国患者的帕金森病建模该怎么做?

      度表达或者敲除 PD 相关蛋白(如 α-突触核蛋白或 LRRK2)来转化目标细胞从而达到模拟病理现象的效果。 但是该模型的一个主要缺点是需要超生理水平的表达相关蛋白才能显现出致病性,这与实际病理现象不符。除此之外,该模型中的 α-突触核蛋白聚集体并不是细丝状,这点特征也与实际病理现象不同。   4.活体注射 α-突触核蛋白模型 该模型是将特定条件下制作的活性蛋白聚集体(aSyn PFFs)注射到活体中来模拟 PD 病理现象。 StressMarq 的活性 aSyn PFFs 在结构功能上都与路易小体中的主要

    图标技术资料

    暂无技术资料 索取技术资料

    同类产品报价

    产品名称
    产品价格
    公司名称
    报价日期
    询价
    上海钰博生物科技有限公司
    2025年06月27日询价
    询价
    上海古朵生物科技有限公司
    2025年07月14日询价
    ¥2400
    深圳市豪地华拓生物科技有限公司
    2025年07月10日询价
    ¥1560
    上海晶抗生物工程有限公司
    2026年03月26日询价
    ¥1180
    上海圻明生物科技有限公司
    2025年07月11日询价
    肌萎缩相关蛋白DAG1抗体
    ¥1900