Anti-NHLRC2 Antibody Picoband® Fluoro594 Conjugated

NHL Repeat Containing Protein 2, or NHLRC2, is a protein encoded by the NHLRC2 gene. NHLRC2 (NHL repeat containing 2) is a 726 amino acid protein that contains six NHL repeats and one thioredoxin domain. Existing as two alternatively spliced isoforms, NHLRC2 is encoded by a gene that maps to human chromosome 10q25.3. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

1. Biterova, E., Ignatyev, A., Uusimaa, J., Hinttala, R., Ruddock, L. W. Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease. PLoS One 13: e0202391, 2018. Note: Electronic Article. 2. Brodsky, N. N., Boyarchuk, O., Kovalchuk, T., Hariyan, T., Rice, A., Ji, W., Khokha, , M., Lakhani, S., Lucas, C. L. Novel compound heterozygous variants in NHLRC2 in a patient with FINCA syndrome. J. Hum. Genet. 65: 911-915, 2020. 3. Gross, M. B. Personal Communication. Baltimore, Md. 1/17/2019.