Bcl-3 Polyclonal Antibody, 20ul Cell Labeling & Imaging Defects in ATG16L1 are a

Defects in ATG16L1 are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10)

It is characterized by short synthesis cycle and is not limited by the source of the template

SLC5A1 (solute carrier family 5 member 1) encodes a member of the sodium-dependent glucose transporter (SGLT) family

MIM 107310) and is required for male fertility and sperm motility (Wang et al

Affected individuals display mottled pigmentation

Bcl-3 Polyclonal Antibody, 20ul Cell Labeling & Imaging Defects in ATG16L1 are aThis gene is a proto oncogene candidate. It is identified by its translocation into the immunoglobulin alpha locus in some cases of B cell leukemia. The protein encoded by this gene contains seven ankyrin repeats, which are most closely related to those found in I kappa B proteins. This protein functions as a transcriptional co activator that activates through its association with NF kappa B homodimers. The expression of this gene can be induced by NF