C7orf43 Antikörper (AA 301-400) (Biotin)
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- Target Alle C7orf43 Produkte
- C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))
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Bindungsspezifität
- AA 301-400
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C7orf43 Antikörper ist konjugiert mit Biotin
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Applikation
- Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
- Homologie
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7ORF43
- Isotyp
- IgG
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- Applikationshinweise
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IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- Haltbarkeit
- 12 months
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- Target
- C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))
- Andere Bezeichnung
- C7ORF43 (C7orf43 Produkte)
- Synonyme
- chromosome 3 open reading frame, human C7orf43 antikoerper, chromosome 7 open reading frame 43 antikoerper, C3H7orf43 antikoerper, c7orf43 antikoerper, C7orf43 antikoerper
- Hintergrund
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Synonyms: C7orf43, CG043_HUMAN, Chromosome 7 open reading frame 43, DKFZp761G0712, FLJ10925, Hypothetical protein LOC55262, Uncharacterized protein C7orf43.
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 C7orf43 gene product has been provisionally designated C7orf43 pending further characterization.
- Gen-ID
- 55262
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