Utrophin anticorps (AA 1211-2294)
Aperçu rapide pour Utrophin anticorps (AA 1211-2294) (ABIN7599842)
Antigène
Voir toutes Utrophin (UTRN) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 1211-2294
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Fonction
- Anti-Utrophin/UTRN Antibody
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Attributs du produit
- Anti-Utrophin/UTRN Antibody. Tested in ELISA, IF, ICC, WB applications. This antibody reacts with Human, Mouse.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human Utrophin/UTRN recombinant protein (Position: L1211-K2294).
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Isotype
- IgG
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Indications d'application
- Western blot, 0.25-0.5 μg/mL, Human, Mouse Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human ELISA, 0.1-0.5 μg/mL, -
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles. -
Date de péremption
- 12 months
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- Utrophin (UTRN)
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Autre désignation
- UTRN
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Sujet
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Background: Utrophin is a protein that in humans is encoded by the UTRN gene. This gene shares both structural and functional similarities with the dystrophin gene. It contains an actin-binding N-terminus, a triple coiled-coil repeat central region, and a C-terminus that consists of protein-protein interaction motifs which interact with dystroglycan protein components. The protein encoded by this gene is located at the neuromuscular synapse and myotendinous junctions, where it participates in post-synaptic membrane maintenance and acetylcholine receptor clustering. Mouse studies suggest that this gene may serve as a functional substitute for the dystrophin gene and therefore, may serve as a potential therapeutic alternative to muscular dystrophy which is caused by mutations in the dystrophin gene. Alternative splicing of the utrophin gene has been described, however, the full-length nature of these variants has not yet been determined.
Gene Full Name: utrophin
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Poids moléculaire
- 394 kDa
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ID gène
- 7402
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UniProt
- P46939
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Pathways
- Skeletal Muscle Fiber Development
Antigène
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