C8orf47 Polyklonale Antilichaam, AbBy FluorTM 555 Vervoeging

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 C8orf47 gene product has been provisionally designated C8orf47 pending further characterization.

C8orf47; CH047_HUMAN; Chromosome 8 open reading frame 47; Uncharacterized protein C8orf47.

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Cytoplasm, Nucleus

Human

1-100/374

C8orf47

AbBy Fluor™ 555

KLH conjugated synthetic peptide derived from human C8orf47

WB

Purified by Protein A.

553nm/568nm

1µg/µl

WB (1:300-5000)

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

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