WebSturge-Weber syndrome. At least one mutation in the GNAQ gene has been found to cause Sturge-Weber syndrome. Sturge-Weber syndrome is a condition that affects the development of certain blood vessels and often leads to three major features: a red or pink birthmark called a port-wine birthmark, brain abnormalities, and increased pressure in the … Web1 2.8123999999999998 3.3220000000000001 3.1793999999999998 5.0674000000000001 3.6124999999999998 3.7989000000000002 4.9747000000000003 4.3353000000000002
TTC39A, Rabbit, Monoclonal Antibody, Abnova 1mg x up to 3 Abs ...
Webttc39a. sections. tissue brain single cell type tissue cell type pathology disease immune cell blood protein subcellular cell line structure metabolic about. introduction history … Web"TTC39A antibodies" comparison. At Proteintech, we pride ourselves on our antibody quality, customer service and transparency. As such, we are comparing our antibodies with other vendors, enabling easy identification and comparisons of key data to help you choose the suitable antibody for your needs. eastman and smith salary
PrEST Antigen TTC39A [Catalog No.: ATL-APrEST76554]
Webttc39a ID ZDB-GENE-091116-42 Name tetratricopeptide repeat domain 39A Symbol ttc39a Nomenclature History Previous Names. si:ch211-77o19.1; si:ch73-22b20.1; Type … WebJun 20, 2014 · Hepatic stellate cells (HSCs) are major players in liver fibrogenesis. Accumulating evidence shows that suppression of autophagy plays an important role in the development and progression of liver disease. Phospholipase D1 (PLD1), which catalyzes the hydrolysis of phosphatidylcholine to yield phosph … WebPrimePCR™ Template for Probe Assay: Ttc39a, Mouse Reaction: 200 x 20 µl reactions Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding probe assay. cultural wilderness