IQCA1 Polyklonale Antilichaam, AbBy FluorTM 647 Vervoeging

The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid 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 due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

IQ and AAA domain-containing protein 1; IQ mot containing with AAA domain 1; IQCA; Iqca1; IQCA1_HUMAN; RGD1305311; FLJ22527; 4930465P12Rik; FLJ33588.

Mouse, Rat

651-750/822

IQCA1

AbBy Fluor™ 647

KLH conjugated synthetic peptide derived from human IQCA1

WB, IF (IHC-P)

Purified by Protein A.

650nm/665nm

1µg/µl

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

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.

Human, Cow, Sheep, Pig, Horse, Rabbit