C12ORF24 Antikörper (AA 195-245) (Biotin)
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- Target Alle C12ORF24 (C12orf24) Produkte
- C12ORF24 (C12orf24) (Chromosome 12 Open Reading Frame 24 (C12orf24))
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Bindungsspezifität
- AA 195-245
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C12ORF24 Antikörper ist konjugiert mit Biotin
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Applikation
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C12ORF24
- Isotyp
- IgG
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- Applikationshinweise
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WB 1:300-5000
IHC-P 1:200-400 - 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
- C12ORF24 (C12orf24) (Chromosome 12 Open Reading Frame 24 (C12orf24))
- Andere Bezeichnung
- C12ORF24 (C12orf24 Produkte)
- Synonyme
- C12orf24 antikoerper, C17H12orf24 antikoerper, HSU79274 antikoerper, 1500011H22Rik antikoerper, family with sequence similarity 216 member A antikoerper, family with sequence similarity 216, member A antikoerper, FAM216A antikoerper, Fam216a antikoerper
- Hintergrund
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Synonyms: Chromosome 12 open reading frame 24, HSU79274, Hypothetical protein LOC29902, Protein predicted by clone 23733, F216A_HUMAN, Protein FAM216A, FAM216A.
Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf24 gene product has been provisionally designated C12orf24 pending further characterization.
- Gen-ID
- 29902
- UniProt
- Q8WUB2
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