DFNB31 Antikörper (AA 708-907)
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- Target Alle DFNB31 Antikörper anzeigen
- DFNB31 (Deafness, Autosomal Recessive 31 (DFNB31))
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Bindungsspezifität
- AA 708-907
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Reaktivität
- Human
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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)
- Sequenz
- PSGHPDQTGT NQHFVMVEVH RPDSEPDVNE VRALPQTRTA STLSQLSDSG QTLSEDSGVD AGEAEASAPG RGRQSVSTKS RSSKELPRNE RPTDGANKPP GLLEPTSTLV RVKKSAATLG IAIEGGANTR QPLPRIVTIQ RGGSAHNCGQ LKVGHVILEV NGLTLRGKEH REAARIIAEA FKTKDRDYID FLVTEFNVML
- Kreuzreaktivität
- Human, Maus
- Produktmerkmale
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 708-907 of human WHRN (NP_056219.3).
- Isotyp
- IgG
- Top Product
- Discover our top product DFNB31 Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000
- Kommentare
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HIGH QUALITY
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- 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)
- Synonyme
- DFNB31 antikoerper, CIP98 antikoerper, PDZD7B antikoerper, USH2D antikoerper, WHRN antikoerper, WI antikoerper, Cip98 antikoerper, Whrn antikoerper, 1110035G07Rik antikoerper, AW122018 antikoerper, AW742671 antikoerper, C430046P22Rik antikoerper, Dfnb31 antikoerper, wi antikoerper, whirlin antikoerper, WHRN antikoerper, LOC100555508 antikoerper, Whrn antikoerper
- Hintergrund
- 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.,WHRN,CIP98,DFNB31,PDZD7B,USH2D,WI,whirlin,Neuroscience,WHRN
- Molekulargewicht
- 37 kDa/55 kDa/59 kDa/96 kDa
- Gen-ID
- 25861
- UniProt
- Q9P202
- Pathways
- Sensory Perception of Sound
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