DOK7 Antikörper (AA 10-90)
Kurzübersicht für DOK7 Antikörper (AA 10-90) (ABIN7221244)
Target
Alle DOK7 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 10-90
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Verwendungszweck
- Dok-7 Polyclonal Antibody
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Spezifität
- Dok-7 Polyclonal Antibody detects endogenous levels of Dok-7 protein.
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Aufreinigung
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the N-terminal region of human Dok-7 at AA range: 10-90
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Isotyp
- IgG
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Applikationshinweise
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), IF (1:200-1:1000), ELISA (1:20000). Not yet tested in other applications.
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Kommentare
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Primary Antibody
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- DOK7 (Docking Protein 7 (DOK7))
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Andere Bezeichnung
- Dok-7
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Hintergrund
- Rabbit Anti-Dok-7 Polyclonal Antibody,DOK7, C4orf25, Protein Dok-7, Downstream of tyrosine kinase 7,The docking protein 7 encoded by DOK7 is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in DOK7 are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants.,Protein Dok-7
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Molekulargewicht
- observerd band 60kDa
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Gen-ID
- 285489
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UniProt
- Q18PE1
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Pathways
- Skeletal Muscle Fiber Development
Target
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