DTNA Antikörper
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- Target Alle DTNA Antikörper anzeigen
- DTNA (Dystrobrevin alpha (DTNA))
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Reaktivität
- Human
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser DTNA Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)
- Produktmerkmale
- Homo sapiens dystrobrevin, alpha (DTNA), transcript variant 5
- Aufreinigung
- Purified from mouse ascites fluids by affinity chromatography
- Immunogen
- Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.
- Klon
- 1B2
- Isotyp
- IgG2a
- Top Product
- Discover our top product DTNA Primärantikörper
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- Applikationshinweise
- WB 1:500~2000, IF 1:100, FLOW 1:100
- Kommentare
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The concentration of the product may vary between diferrent lots.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
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- Target
- DTNA (Dystrobrevin alpha (DTNA))
- Andere Bezeichnung
- DTNA (DTNA Produkte)
- Synonyme
- adtn antikoerper, atnb antikoerper, MGC146484 antikoerper, 2210407P21Rik antikoerper, A0 antikoerper, Dtn antikoerper, a-DB-1 antikoerper, adbn antikoerper, D18S892E antikoerper, DRP3 antikoerper, DTN antikoerper, DTN-A antikoerper, LVNC1 antikoerper, Dtna-ps1 antikoerper, RGD1561985 antikoerper, dystrobrevin alpha antikoerper, dystrobrevin, alpha antikoerper, DTNA antikoerper, dtna antikoerper, LOC100195747 antikoerper, Dtna antikoerper
- Hintergrund
- The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
- Molekulargewicht
- 58.7 kDa
- Gen-ID
- 1837
- NCBI Accession
- NM_032979
- HGNC
- 1837
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