OTOA Antikörper (N-Term)
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- Target Alle OTOA Antikörper anzeigen
- OTOA (Otoancorin (OTOA))
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Bindungsspezifität
- AA 99-127, N-Term
- Reaktivität
- Maus, Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser OTOA Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
- Spezifität
- This antibody recognizes Human and Mouse Otoancorin / OTOA (N-term).
- Aufreinigung
- Protein A column, followed by peptide affinity purification
- Immunogen
- KLH conjugated synthetic peptide between 99-127 amino acids from the N-terminal region of human Otoancorin / OTOA
- Isotyp
- Ig Fraction
- Top Product
- Discover our top product OTOA Primärantikörper
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- Applikationshinweise
- Optimal working dilution should be determined by the investigator.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 0.25 mg/mL
- Buffer
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handhabung
- Avoid repeated freezing and thawing.
- Lagerung
- 4 °C/-20 °C
- Informationen zur Lagerung
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Target
- OTOA (Otoancorin (OTOA))
- Andere Bezeichnung
- Otoancorin / OTOA (OTOA Produkte)
- Synonyme
- CT108 antikoerper, DFNB22 antikoerper, RGD1562741 antikoerper, otoancorin antikoerper, otoancorin L homeolog antikoerper, OTOA antikoerper, otoa.L antikoerper, otoa antikoerper, Otoa antikoerper
- Hintergrund
- The protein encoded by this gene is specifically expressed in the inner ear, and is located at the interface between the apical surface of the inner ear sensory epithelia and their overlying acellular gels. It is prposed that this protein is involved in the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in this gene are associated with autosomal recessive deafness type 22 (DFNB22). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].
- Molekulargewicht
- 128533 Da
- Gen-ID
- 146183
- NCBI Accession
- NP_001155155
- Pathways
- Sensory Perception of Sound
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