C22orf9 antibody (AbBy Fluor® 350)
-
- Target See all C22orf9 products
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
-
Reactivity
- Human, Mouse, Rat
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This C22orf9 antibody is conjugated to AbBy Fluor® 350
-
Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C22orf9
- Isotype
- IgG
-
-
- Application Notes
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
-
- 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.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
-
- Target
- C22orf9 (Chromosome 22 Open Reading Frame 9 (C22orf9))
- Alternative Name
- C22orf9 (C22orf9 Products)
- Synonyms
- c22orf9 antibody, C22orf9 antibody, AW554572 antibody, mKIAA0930 antibody, KIAA0930 S homeolog antibody, KIAA0930 antibody, RIKEN cDNA 5031439G07 gene antibody, similar to CG9646-PA antibody, KIAA0930 ortholog antibody, kiaa0930.S antibody, KIAA0930 antibody, kiaa0930 antibody, 5031439G07Rik antibody, RGD1304694 antibody, Kiaa0930 antibody
- Background
-
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.
- Gene ID
- 23313
-