Cadherin-19 Polyclonal Antibody, 100ul Glassware Sets Mutations in SLC24A1 may play

Mutations in SLC24A1 may play a role in congenital stationary night blindness

Proteins modified in this way

a multisystem developmental disorder caused by deletion of multiple genes at 7q11

and is safe and convenient to use

Rab GTPases are active

Cadherin-19 Polyclonal Antibody, 100ul Glassware Sets Mutations in SLC24A1 may playCDH19 is one of three related type II cadherin genes situated in a cluster on chromosome 18. The encoded protein (cadherin 19) is a calcium dependent cell cell adhesion glycoprotein containing five extracellular cadherin repeats. Loss of cadherins may be associated with cancer formation. Alternative splicing results in multiple transcript variants for CDH19.