Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc Alpha receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf26 gene product has been provisionally designated C19orf26 pending further characterization.

Chromosome 19 open reading frame 26;
C19orf26;
DOS;
Protein Dos;
CBARP_HUMAN;
Voltage-dependent calcium channel beta subunit-associated regulatory protein;CACN Subunit Beta Associated Regulatory Protein; Calcium Channel, Voltage-Dependent, Beta Subunit Associated Regulatory Protein;
CACN Beta Subunit Associated Regulatory Protein;VGCC Beta-Anchoring And -Regulatory Protein;Downstream Of STK11;Downstream Of Stk11;CBARP.

Human,Mouse,Rat

IHC,IF,ICC,ELISA

IHC 1:50-1:200
IF 1:100-500
ICC 1:100-1:400
ELISA 1:5000-10000

74kD

255057

Q8N350

https://www.uniprot.org/uniprotkb/Q8N350

Membrane.

KLH conjugated synthetic peptide derived from human CBARP

Rabbit

Polyclonal

IgG

affinity purified by Protein A

Liquid

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

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