DFNA5 Antikörper
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- Target Alle DFNA5 Antikörper anzeigen
- DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
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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 DFNA5 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human DFNA5
- Isotyp
- IgG
- Top Product
- Discover our top product DFNA5 Primärantikörper
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- Applikationshinweise
- WB 1:500 - 1:2000 IHC 1:50 - 1:200
- 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
- DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
- Andere Bezeichnung
- DFNA5 (DFNA5 Produkte)
- Synonyme
- Dfna5h antikoerper, fk59f08 antikoerper, zgc:91916 antikoerper, wu:fc41e05 antikoerper, wu:fk59f08 antikoerper, MGC83660 antikoerper, ICERE-1 antikoerper, 2310037D07Rik antikoerper, 4932441K13Rik antikoerper, EG14210 antikoerper, Fin15 antikoerper, gasdermin E antikoerper, gasdermin Eb antikoerper, DFNA5, deafness associated tumor suppressor antikoerper, gasdermin E L homeolog antikoerper, Gsdme antikoerper, gsdmeb antikoerper, DFNA5 antikoerper, gsdme.L antikoerper, GSDME antikoerper
- Hintergrund
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Synonyms: 2310037D07Rik,4932441K13Rik,Deafness,autosomal dominant 5,Deafness,autosomal dominant 5 protein,DFNA5,DFNA5 gene,DFNA5,Dfna5h,EG14210,Fin15,ICERE 1,ICERE-1,Inversely correlated with estrogen receptor expression 1,Non-syndromic hearing impairment protein 5,Nonsyndromic hearing impairment protein
Background: Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.
- Molekulargewicht
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Observed_MW: 50kDa
Calculated_MW: 10kDa/36kDa/54kDa
- Gen-ID
- 1687
- UniProt
- O60443
- Pathways
- Sensory Perception of Sound
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