HMGB3 Rabbit Polyclonal Antibody, 50ul Cell Culture Flasks Unleash the power of LightNing™

Unleash the power of LightNing™ NcoI Restriction Enzymes

The gene is deleted in Williams-Beuren syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11

IFNG encodes a soluble cytokine that is a member of the type II interferon class

a transcriptional regulator of immunoglobulin genes

with structural similarity to the immunoglobulin variable domains

HMGB3 Rabbit Polyclonal Antibody, 50ul Cell Culture Flasks Unleash the power of LightNing™This gene encodes a member of a family of proteins containing one or more high mobility group DNA binding motifs. The encoded protein plays an important role in maintaining stem cell populations and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants.