OSTM1 Antikörper
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- Target Alle OSTM1 Antikörper anzeigen
- OSTM1 (Osteopetrosis Associated Transmembrane Protein 1 (OSTM1))
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Reaktivität
- Human, Ratte, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser OSTM1 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human OSTM1
- Isotyp
- IgG
- Top Product
- Discover our top product OSTM1 Primärantikörper
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- Applikationshinweise
- WB 1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 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
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- OSTM1 (Osteopetrosis Associated Transmembrane Protein 1 (OSTM1))
- Andere Bezeichnung
- OSTM1 (OSTM1 Produkte)
- Synonyme
- MGC145644 antikoerper, si:ch73-257c13.3 antikoerper, GIPN antikoerper, GL antikoerper, OPTB5 antikoerper, 1200002H13Rik antikoerper, HSPC019 antikoerper, gl antikoerper, Gipn antikoerper, OSTM1 antikoerper, osteopetrosis associated transmembrane protein 1 antikoerper, OSTM1 antikoerper, ostm1 antikoerper, Ostm1 antikoerper
- Hintergrund
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Synonyms: Chloride channel 7 beta subunit,GAIP-interacting protein N terminus,GIPN,GL,Grey lethal osteopetrosis,HSPC019,OPTB5,Osteopetrosis-associated transmembrane protein 1,Ostm1,OSTM1,OTTHUMP00000016938,OTTHUMP00000196342
Background: This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis.
- Molekulargewicht
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Observed_MW: 37kDa
Calculated_MW: 37kDa
- Gen-ID
- 28962
- UniProt
- Q86WC4
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