C21ORF62 Polyklonale Antilichaam, PE-vervoeging

The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. The C21orf62 gene product has been provisionally designated C21orf62 pending further characterization.

B37; C21orf120; Chromosome 21 open reading frame 62; Hypothetical protein LOC56245; PRED81; Uncharacterized protein C21orf62; CU062_HUMAN.

56245

Human, Mouse, Rat

51-150/219

C21ORF62

PE

KLH conjugated synthetic peptide derived from human C21ORF62

WB, IF

Purified by Protein A.

496,564nm/578nm

1µg/µl

WB (WB=1:500-2000), IF (IF=1:100-500)

Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

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

56245