USH1G Antikörper
USH1G
Reaktivität: Human
ELISA, IP
Wirt: Kaninchen
Polyclonal
unconjugated
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- Target Alle USH1G Antikörper anzeigen
- USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser USH1G Antikörper ist unkonjugiert
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Applikation
- ELISA, Immunoprecipitation (IP)
- Aufreinigung
- Immunogen affinity purified
- Reinheit
- ≥95 % as determined by SDS-PAGE
- Immunogen
- Usher syndrome 1G(autosomal recessive)
- Isotyp
- IgG
- Top Product
- Discover our top product USH1G Primärantikörper
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- Applikationshinweise
- IP: 1:200-1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide and 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
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
- Haltbarkeit
- 12 months
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- Target
- USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
- Andere Bezeichnung
- USH1G (USH1G Produkte)
- Hintergrund
- Synonyms:ANKS4A, FLJ33924, SANS, USH1G, Usher syndrome type 1G protein Background:Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.
- Molekulargewicht
- 52 kDa
- Gen-ID
- 124590
- UniProt
- Q495M9
- Pathways
- Sensory Perception of Sound
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