DFNB31 Antikörper
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- Target Alle DFNB31 Antikörper anzeigen
- DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
- Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser DFNB31 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human WHRN
- Isotyp
- IgG
- Top Product
- Discover our top product DFNB31 Primärantikörper
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anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 378-406) antibody
DFNB31 Reaktivität: Human WB, IHC (p) Wirt: Kaninchen Polyclonal RB19059 unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 808-907) antibodyDFNB31 Reaktivität: Human WB, ELISA Wirt: Maus Monoclonal 1D9 unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 808-907) antibodyDFNB31 Reaktivität: Human WB, ELISA, IF Wirt: Maus Monoclonal 2D12 unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 808-907) antibodyDFNB31 Reaktivität: Human WB, ELISA Wirt: Maus Polyclonal unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 708-907) antibodyDFNB31 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
anti-Deafness, Autosomal Recessive 31 (DFNB31) (AA 385-413), (Middle Region) antibodyDFNB31 Reaktivität: Human WB, IHC (p), EIA Wirt: Kaninchen Polyclonal unconjugated
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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
- DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
- Andere Bezeichnung
- WHRN (DFNB31 Produkte)
- Hintergrund
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Synonyms: Whirlin,Autosomal Recessive Deafness Type 31 Protein,DFNB31,Deafness Autosomal Recessive 31,CASK-Interacting Protein CIP98,KIAA1526,PDZD7B,CIP98,USH2D,WI,WHRN,KIAA1526
Background: This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants.
- Molekulargewicht
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Observed_MW: 110kDa
Calculated_MW: 37kDa/55kDa/59kDa/96kDa
- Gen-ID
- 25861
- UniProt
- Q9P202
- Pathways
- Sensory Perception of Sound
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