C22orf9 anticorps (AbBy Fluor® 750)
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- Antigène Tous les produits C22orf9
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C22orf9 est conjugé à/à la AbBy Fluor® 750
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C22orf9
- Isotype
- IgG
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- Indications d'application
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
- Autre désignation
- C22orf9 (C22orf9 Produits)
- Synonymes
- anticorps c22orf9, anticorps C22orf9, anticorps AW554572, anticorps mKIAA0930, anticorps KIAA0930 S homeolog, anticorps KIAA0930, anticorps RIKEN cDNA 5031439G07 gene, anticorps similar to CG9646-PA, anticorps KIAA0930 ortholog, anticorps kiaa0930.S, anticorps KIAA0930, anticorps kiaa0930, anticorps 5031439G07Rik, anticorps RGD1304694, anticorps Kiaa0930
- Sujet
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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.
- ID gène
- 23313
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