Laminin anticorps (AA 152-170)

N° du produit ABIN3029737

Cet anticorps Lapin Polyclonal détecte spécifiquement Laminin dans WB. Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour Laminin anticorps (AA 152-170) (ABIN3029737)

Antigène: Laminin (LAMA2) (Laminin, alpha 2 (LAMA2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Laminin est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Laminin anticorps

Épitope: AA 152-170

Purification: Antigen affinity

Immunogène: Amino acids 152-170 (WILERSLDDVEYKPWQYHA-human) were used as the immunogen for this LAMA2 antibody (100% mouse homology).

Isotype: IgG

Information d'application

Indications d'application: The stated application concentrations are suggested starting points. Titration of the LAMA2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 0.5-1 μg/mL

Restrictions: For Research Use only

Stockage

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: -20 °C

Stockage commentaire: After reconstitution, the LAMA2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Détails sur Laminin

Antigène: Laminin (LAMA2) (Laminin, alpha 2 (LAMA2))

Autre désignation: LAMA2 Laminin 2 alpha

Sujet: Laminin 2 alpha is a protein that in humans is encoded by the LAMA2 gene. This gene is mapped to 6q22.33. Laminin, an extracellular protein, is a major component of the basement membrane. It is though 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.

UniProt: P24043