C22orf9 Antikörper (AbBy Fluor® 594)
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- Target Alle C22orf9 Produkte
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
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Reaktivität
- Maus, Ratte, Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser C22orf9 Antikörper ist konjugiert mit AbBy Fluor® 594
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Applikation
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C22orf9
- Isotyp
- IgG
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- Applikationshinweise
- IF(IHC-P) 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
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
- Andere Bezeichnung
- C22orf9 (C22orf9 Produkte)
- Synonyme
- c22orf9 antikoerper, C22orf9 antikoerper, AW554572 antikoerper, mKIAA0930 antikoerper, KIAA0930 S homeolog antikoerper, KIAA0930 antikoerper, RIKEN cDNA 5031439G07 gene antikoerper, similar to CG9646-PA antikoerper, KIAA0930 ortholog antikoerper, kiaa0930.S antikoerper, KIAA0930 antikoerper, kiaa0930 antikoerper, 5031439G07Rik antikoerper, RGD1304694 antikoerper, Kiaa0930 antikoerper
- Hintergrund
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Synonyms: Chromosome 22 open reading frame 9, Hypothetical protein LOC23313, KIAA0930, Uncharacterized protein C22orf9, K0930_HUMAN.
Background: C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
- Gen-ID
- 23313
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