Utrophin Antikörper (AA 1211-2294)
Kurzübersicht für Utrophin Antikörper (AA 1211-2294) (ABIN8052949)
Target
Alle Utrophin (UTRN) Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
Güteklasse
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Bindungsspezifität
- AA 1211-2294
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Verwendungszweck
- Anti-Utrophin/UTRN Antibody
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Kreuzreaktivität (Details)
- No cross-reactivity with other proteins.
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Produktmerkmale
- Anti-Utrophin/UTRN Antibody. Tested in ELISA, IF, ICC, WB applications. This antibody reacts with Human, Mouse.
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Aufreinigung
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human Utrophin/UTRN recombinant protein (Position: L1211-K2294).
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Isotyp
- IgG
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Applikationshinweise
- 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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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Konzentration
- 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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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
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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. -
Haltbarkeit
- 12 months
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- Utrophin (UTRN)
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Andere Bezeichnung
- UTRN
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Hintergrund
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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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Molekulargewicht
- 394 kDa
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Gen-ID
- 7402
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UniProt
- P46939
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Pathways
- Skeletal Muscle Fiber Development
Target
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