C1orf181 Polyclonal Antibody, 50ul Transporters Mutations in this gene are

Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC

VitroGel® MMP High Concentration comes with VitroGel® Dilution Solution (contains sucrose for best osmolarity) to adjust the final hydrogel strength from 10 to 4000 Pa

TARC and MCP-1

Shows affinity for calcium and barium ions

The protein encoded by KCNJ5 is an integral membrane protein and inward-rectifier type potassium channel

C1orf181 Polyclonal Antibody, 50ul Transporters Mutations in this gene areZNHIT6 (Zinc Finger HIT Type Containing 6) is a Protein Coding gene. GO annotations related to this gene include identical protein binding and enzyme binding.