NBR1 mouse Monoclonal Antibody(7C3), 100ul Vector Construction Not detected in liver

Not detected in liver

and better sample processing effect

This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS)

The reversible posttranslational modification of proteins by the addition of small ubiquitin-like SUMO proteins (see SUMO1

Chondroitin sulfate constitutes the predominant proteoglycan present in cartilage

NBR1 mouse Monoclonal Antibody(7C3), 100ul Vector Construction Not detected in liverThe protein encoded by this gene was originally identified as an ovarian tumor antigen monitored in ovarian cancer. The encoded protein contains a B box coiled coil motif, which is present in many genes with transformation potential. It functions as a specific autophagy receptor for the selective autophagic degradation of peroxisomes by forming intracellular inclusions with ubiquitylated autophagic substrates. This gene is located on a region of