C7ORF26 Antikörper (AA 1-100) (Cy5)
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- Target Alle C7ORF26 Produkte
- C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))
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Bindungsspezifität
- AA 1-100
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C7ORF26 Antikörper ist konjugiert mit Cy5
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Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Homologie
- Human,Mouse,Rat,Dog,Cow,Chicken,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7orf26
- Isotyp
- IgG
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- Applikationshinweise
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))
- Andere Bezeichnung
- C7orf26 (C7ORF26 Produkte)
- Synonyme
- C14H7orf26 antikoerper, zgc:77458 antikoerper, c7orf26 antikoerper, chromosome 7 open reading frame 26 antikoerper, chromosome 14 C7orf26 homolog antikoerper, zgc:56409 antikoerper, chromosome 7 open reading frame 26 L homeolog antikoerper, chromosome 25 open reading frame, human C7orf26 antikoerper, C7orf26 antikoerper, C14H7orf26 antikoerper, zgc:56409 antikoerper, c7orf26.L antikoerper, C25H7orf26 antikoerper
- Hintergrund
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Synonyms: Chromosome 7 open reading frame 26, MGC2718, Uncharacterized protein C7orf26,CG026_HUMAN.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterization.
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