C7ORF25 Antikörper (AA 1-100) (Biotin)
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- Target Alle C7ORF25 Produkte
- C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))
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Bindungsspezifität
- AA 1-100
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Reaktivität
- Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C7ORF25 Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Kreuzreaktivität
- Maus
- Homologie
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C7orf25
- Isotyp
- IgG
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- Applikationshinweise
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WB 1:300-5000
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
- C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))
- Andere Bezeichnung
- C7orf25 (C7ORF25 Produkte)
- Synonyme
- C7orf25 antikoerper, c7orf25 antikoerper, chromosome 7 open reading frame 25 antikoerper, chromosome 4 open reading frame, human C7orf25 antikoerper, expressed sequence AW209491 antikoerper, similar to expressed sequence AW209491 antikoerper, chromosome 7 open reading frame 25 L homeolog antikoerper, C7orf25 antikoerper, C4H7orf25 antikoerper, AW209491 antikoerper, RGD1308147 antikoerper, c7orf25.L antikoerper
- Hintergrund
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Synonyms: C7orf25, CG025_HUMAN, Chromosome 7 open reading frame 25, RGD1308147, UPF0415 protein C7orf25.
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 C7orf25 gene product has been provisionally designated C7orf25 pending further characterization.
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