HSP70 Monoclonal Antibody(3G10), 100ul Custom Peptide Synthesis Mutations in OCRL cause oculocerebrorenal

Mutations in OCRL cause oculocerebrorenal syndrome of Lowe and also Dent disease

CDC37L1 is a cytoplasmic phosphoprotein that exists in complex with HSP90 (HSPCA

This complex is critical for accurate chromosome alignment and segregation and it ensures proper mitotic progression

With 10g of potency and a high concentration of 175KU/mL

which is required for normal postnatal growth and survival

HSP70 Monoclonal Antibody(3G10), 100ul Custom Peptide Synthesis Mutations in OCRL cause oculocerebrorenalThis gene encodes a 70kDa heat shock protein. In conjunction with other heat shock proteins, this protein stabilizes existing proteins against aggregation and mediates the folding of newly translated proteins in the cytosol and in organelles. The gene is located in the major histocompatibility complex class III region, in a cluster with two closely related genes which also encode isoforms of the 70kDa heat shock protein.