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Laminin α-2 Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-72524

  • Amount:

    100ul

  • Applications:

    IHC-p;IF/ICC;ELISA

  • Reactivity:

    Human;Mouse

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human LAMA2. AA range:2011-2060

  • Source:

    Polyclonal, Rabbit

  • Gene Name:

    LAMA2

  • Dilution:

    Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.

  • Immunohistochemistry analysis of paraffin-embedded human placenta tissue, using LAMA2 Antibody. The picture on the right is blocked with the synthesized peptide.

  • Background:

    laminin subunit alpha 2(LAMA2) Homo sapiens Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Jul 2008],

  • Protein Name:

    Laminin subunit alpha-2

  • Human Gene Id:

    3908

  • Human Swiss Prot No:

    P24043

  • Mouse Swiss Prot No:

    Q60675

  • Specificity:

    Laminin α-2 Polyclonal Antibody detects endogenous levels of Laminin α-2 protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    LAMA2; LAMM; Laminin subunit alpha-2; Laminin M chain; Laminin-12 subunit alpha; Laminin-2 subunit alpha; Laminin-4 subunit alpha; Merosin heavy chain

  • MolecularWeight(Da):

    342771

  • Function:

    disease:Defects in LAMA2 are the cause of merosin-deficient congenital muscular dystrophy type 1A (MDC1A) [MIM:607855]. MDC1A is characterized by difficulty walking, hypotonia, proximal weakness, hyporeflexia, and white matter hypodensity on MRI.,domain:Domains VI, IV and G are globular.,domain:The alpha-helical domains I and II are thought to interact with other laminin chains to form a coiled coil structure.,function: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.,similarity:Contains 1 laminin N-terminal domain.,similarity:Contains 17 laminin EGF-like domains.,similarity:Contains 2 laminin IV type A domains.,similarity:Contains 5 laminin G-like domains.,subcellular location:Major component.,subunit:Laminin

  • Subcellular Location:

    extracellular region,basement membrane,basal lamina,extracellular matrix,sarcolemma,dendritic spine,extracellular exosome,

  • Expression:

    Brain,Liver,Placenta,Plasma,

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Catalog Number

  • Amount:100ul
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Laminin α-2 Polyclonal Antibody | EnoGene Biotech Co. Ltd