DLEC1 Polyclonal Antibody, 20ul Custom DNA Oligos Mutations in CTSD play a

Mutations in CTSD play a causal role in neuronal ceroid lipofuscinosis-10 and may be involved in the pathogenesis of several other diseases

Stickler syndrome type I

This receptor shows high affinity for corticotropin releasing hormone (CRH)

Mutations in this gene are associated with type IIA autoimmune lymphoproliferative syndrome

such as cocaine and heroin

DLEC1 Polyclonal Antibody, 20ul Custom DNA Oligos Mutations in CTSD play aThe cytogenetic location of DLEC1 (deleted in lung and esophageal cancer 1) is 3p21. , and it is located in a region that is commonly deleted in a variety of malignancies. Down regulation of DLEC1 has been observed in several human cancers including lung, esophageal, renal tumors, and head and neck squamous cell carcinoma. In some cases, reduced expression of DLEC1 in tumor cells is a result of aberrant promoter methylation. Several alternatively