BCAS3 Polyclonal Antibody, 100ul Electrophoresis & Labeling HLX is a Protein Coding

HLX is a Protein Coding gene

and mutations in this gene are a cause of hereditary leukonychia

It is also involved in the maintenance of chromatin structure

Mutations in this gene are associated with stress-induced polymorphic ventricular tachycardia and arrhythmogenic right ventricular dysplasia

BCAS3 Polyclonal Antibody, 100ul Electrophoresis & Labeling HLX is a Protein CodingRudhira BCAS3 (Breast Cancer Amplified Sequence 3) is a conserved protein expressed in the embryonic vasculature and malignant tumors. Rudhira is a predicted WD40 domain protein. During mouse development Rudhira is expressed in erythropoietic and angiogenic precursors but not in their differentiated progeny. This transient expression of Rudhira is also seen in normal adult angiogenesis. BCAS3, the human ortholog of Rudhira is 98% identical and the