0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
0.62mg/ml(Please refer to the vial label for the specific concentration.)
Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human NTAL. The exact sequence is proprietary.
Purified by antigen-affinity chromatography.
For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
LAB antibody, NTAL antibody, WBSCR15 antibody, WBSCR5 antibody, WSCR5 antibody, LAT2 antibody, linker for activation of T-cells family member 2 antibody, membrane-associated adapter molecule antibody, "linker for activation of T cells, transmembrane adaptor 2 antibody", non-T-cell activation linker antibody, Williams-Beuren syndrome chromosomal region 15 protein antibody, Williams-Beuren syndrome chromosomal region 5 protein antibody, linker for activation of B-cells antibody, "linker for activation of T cells family, member 2 antibody"
Cell membrane; Single-pass type III membrane protein
This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq]