C2orf68 Polyklonale Antilichaam

C2orf68, also known as FLJ14112, FLJ35653 or MGC131675, is a 168 amino acid protein belonging to the UPF0561 family. Existing as two alternatively spliced isoforms, C2orf68 is encoded by a gene that maps to human chromosome 2q11.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

Chromosome 2 open reading frame 68; FLJ14112; FLJ35653; MGC131675; CB068_HUMAN.

1-100/166

C2orf68

Unconjugated

KLH conjugated synthetic peptide derived from human C2orf68

WB, IHC-P, IF (IHC-P)

Purified by Protein A.

1µg/µl

WB (1:300-5000), IHC-P (1:200-400), IF (IHC-P) (1:50-200)

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

Unmodified

Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Human, Mouse, Rat, Dog, Cow, Sheep, Pig, Horse, Rabbit