• merck millipore,默克密理博,MAB1905,Anti-Laminin α1/β 1 Antibody, clone AL-4
  • merck millipore,默克密理博,MAB1905,Anti-Laminin α1/β 1 Antibody, clone AL-4

    产品名称:Anti-Laminin α1/β 1 Antibody, clone AL-4
    产品型号:MAB1905
    This Anti-Laminin α1/β 1 Antibody, clone AL-4 is validated for use in ELISA, IP, WB, IH(P) for the detection of Laminin α1/β 1.

    merck millipore,默克密理博,MAB1905,Anti-Laminin α1/β 1 Antibody, clone AL-4

  • 产品介绍
  • merck millipore,默克密理博,MAB1905,Anti-Laminin α1/β 1 Antibody, clone AL-4

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    MWB, ELISARPurifiedMonoclonal Antibody
    描述
    产品目录编号 MAB1905
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-Laminin α1/β 1 Antibody, clone AL-4
    Alternate Names
    • Laminin A Chain
    产品信息
    格式 Purified
    演示 Purified from ascites by Protein G affinity chromatography. Purified immunoglobulin in 0.02M PB, 0.25M NaCl, pH=7.6, 0.1% sodium azide
    应用
    应用 This Anti-Laminin α1/β 1 Antibody, clone AL-4 is validated for use in ELISA, IP, WB, IH(P) for the detection of Laminin α1/β 1.
    主要应用
    • Western Blotting
    • ELISA
    应用说明 ELISA/RIA

    Western blot

    Immunoprecipitation

    Immunohistochemistry. Reactive on tissue frozen in OCT at -70°C. Sections may be treated with hyaluronidase. Shows reactivity to paraffin embedded EHS tumor.

    Optimal working dilutions must be determined by the end user.
    生物信息
    免疫原品种 Laminin isolated from mouse EHS tumor.
    克隆 AL-4
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Rat
    特异性 As original characterized, clone AL-4 reacts with EHS mouse laminin, A chain (laminin α1). The epitope is mapped to the carboxy terminal globular domain on the A chain. Recent work by Scheele et al (2006) has further demonstrated that clone AL-4, under reducing conditions, recognized both the 200 kDa β1/γ1 band and the 400 kDa α1 band of mouse EHS laminin. However the affinity for the 400 kDa band was very low. AL-4 also demonstrated strong binding the Laminin β1. By ELISA the epitope for the AL-4 seemed to be located on the Laminin β1 chain, however the clone also recognizes the laminin α1 chain in immunoblots, thus AL-4 seems to show mixed cross reactivity to laminins α1 and β1, with the β1 reactivity being more prominent.
    同种型 IgG
    品种反应性 Mouse
    抗体类型 Monoclonal Antibody
    Entrez基因编号
    • NM_005559.2
    基因符号
    • LAMA
    • LAMA1
    UniProt编号
    • P55268
    • P25391
    UniProt汇总 FUNCTION: SwissProt: P55268 # Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.
    SIZE: 1798 amino acids; 195981 Da
    SUBUNIT: Laminin is a complex glycoprotein, consisting of three different polypeptide chains (alpha, beta, gamma), which are bound to each other by disulfide bonds into a cross-shaped molecule comprising one long and three short arms with globules at each end. Beta-2 is a subunit of laminin-3 (S-laminin), laminin-4 (S- merosin), and laminin-7 (KS-laminin).
    SUBCELLULAR LOCATION: Secreted, extracellular space. Note=S- laminin is concentrated in the synaptic cleft of the neuromuscular junction.
    DOMAIN: SwissProt: P55268 The alpha-helical domains I and II are thought to interact with other laminin chains to form a coiled coil structure. & Domains VI and IV are globular.
    DISEASE: SwissProt: P55268 # Defects in LAMB2 are the cause of Pierson syndrome [MIM:609049]; also known as microcoria-congenital nephrotic syndrome. Pierson syndrome is characterized by nephrotic syndrome with neonatal onset, diffuse mesangial sclerosis and eye abnormalities with microcoria as the leading clinical feature. Death usually occurs within the first weeks of life. Disease severity depends on the mutation type: nontruncating LAMB2 mutations may display variable phenotypes ranging from a milder variant of Pierson syndrome to isolated congenital nephrotic syndrome. & Defects in LAMB2 are a cause of congenital nephrotic syndrome [MIM:609049]. Congenital nephrotic syndrome constitutes a heterogeneous group of conditions having in common the disruption of normal glomerular permselectivity. Congenital nephrotic syndrome due to LAMB2 mutations may be associated with ocular abnormalities.
    SIMILARITY: Contains 13 laminin EGF-like domains. & Contains 1 laminin IV type B domain. & Contains 1 laminin N-terminal domain.
    产品使用声明
    使用声明
    • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
    储存和货运信息
    存储条件 Maintain between 2 and 8°C.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,MAB1905,Anti-Laminin α1/β 1 Antibody, clone AL-4

上一件merck millipore产品:merck millipore,默克密理博,ABE91,Anti-JMJD8 Antibody
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