C8orf45 Rabbit Polyclonal Antibody
No Size Price Availability  
YRP15298-01 50ul 1500.00 In Stock
YRP15298-01 100ul 2000.00 In Stock
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Source: Rabbit Gene Id: 157777
Isotype: IgG Swiss Prot:
purity: Purified by Protein A.
Background:
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf45 gene product has been provisionally designated C8orf45 pending further characterization.
Reactivity Human, Mouse, Rat
Tested applications WB IHC IF
Clonality Polyclonal Antibody
Calculated MW /
Recommended Dilutions
WB 1:100-1:1000
IHC 1:100-1:500
IF 1:50-1:200
Immunogen KLH conjugated synthetic peptide derived from human C8orf45
Storage Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at -20℃ for 12 months
Synonym C8orf45, Chromosome 8 open reading frame 45, FLJ25692, Minichromosome maintenance complex component like, Uncharacterized protein C8orf45, MCMD2_HUMAN.
This product is for research use only, not for diagnostic or therapeutic use!

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