Gephyrin Antikörper
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- Target Alle Gephyrin (GPHN) Antikörper anzeigen
- Gephyrin (GPHN)
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Reaktivität
- Human
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser Gephyrin Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF)
- Produktmerkmale
- Homo sapiens gephyrin (GPHN), transcript variant 1
- Aufreinigung
- Purified from mouse ascites fluids by affinity chromatography
- Immunogen
- Full length human recombinant protein of human GPHN(NP_065857)
- Klon
- 5B6
- Isotyp
- IgG2a
- Top Product
- Discover our top product GPHN Primärantikörper
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- Applikationshinweise
- WB 1:2000, 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
- Gephyrin (GPHN)
- Andere Bezeichnung
- GPHN (GPHN Produkte)
- Synonyme
- 5730552E08Rik antikoerper, AI662856 antikoerper, BC027112 antikoerper, C230040D23 antikoerper, GPH antikoerper, GPHRYN antikoerper, geph antikoerper, Geph antikoerper, GPHN antikoerper, GEPH antikoerper, HKPX1 antikoerper, gpgb1 antikoerper, DKFZp459M0825 antikoerper, gephyrin antikoerper, gephyrin L homeolog antikoerper, gephyrin a antikoerper, Gphn antikoerper, GPHN antikoerper, gphn.L antikoerper, gphna antikoerper, PTRG_08978 antikoerper, VDBG_00775 antikoerper, Tsp_03043 antikoerper, gphn antikoerper
- Hintergrund
- This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described, however, the full-length nature of all transcript variants is not currently known.
- Molekulargewicht
- 83.3 kDa
- Gen-ID
- 10243
- NCBI Accession
- NM_020806
- HGNC
- 10243
- Pathways
- Synaptic Membrane, Skeletal Muscle Fiber Development
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