ITGA7 anticorps (AA 229-257)
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- Antigène Voir toutes ITGA7 Anticorps
- ITGA7 (Integrin, alpha 7 (ITGA7))
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Épitope
- AA 229-257
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp ITGA7 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Réactivité croisée (Details)
- Expected species reactivity: Mouse
- Purification
- Antigen affinity purified
- Immunogène
- A portion of amino acids 229-257 from the human protein was used as the immunogen for this Integrin alpha 7 antibody.
- Isotype
- Ig Fraction
- Top Product
- Discover our top product ITGA7 Anticorps primaire
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- Indications d'application
- Titration of the Integrin alpha 7 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- In 1X PBS, pH 7.4, with 0.09 % sodium azide
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Aliquot the Integrin alpha 7 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
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- Antigène
- ITGA7 (Integrin, alpha 7 (ITGA7))
- Autre désignation
- Integrin alpha 7 (ITGA7 Produits)
- Synonymes
- anticorps [a]7, anticorps alpha7, anticorps integrin alpha 7, anticorps integrin subunit alpha 7, anticorps Itga7, anticorps ITGA7
- Sujet
- The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
- UniProt
- Q13683
- Pathways
- Integrin Complex
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