TM138抗体应用：WB 1:500-2000 This gene encodes a multi-pass transmembrane protein. Reduced expression of this gene in mouse fibroblasts causes short cilia and failure of ciliogenesis. Expression of this gene is tightly coordinated with expression of the neighboring gene TMEM216. Mutations in this gene are associated with the autosomal recessive neurodevelopmental disorder Joubert Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012],

TM141抗体应用：IHC-p 1：50-200

TM144抗体应用：WB 1:500-2000

TM14A抗体应用：IHC-p 1：50-200

TM169抗体应用：WB 1:500-2000

TM171抗体应用：WB 1:500-2000 ELISA 1:5000-20000TMEM171 (Transmembrane Protein 171) is a Protein Coding gene.

TM1L1抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Probable adapter protein involved in signaling pathways. Interacts with the SH2 and SH3 domains of various signaling proteins when it is phosphorylated. May promotes FYN activation, possibly by disrupting intramolecular SH3-dependent interactions.,PTM:Phosphorylated on tyrosines by FYN (By similarity). Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the TOM1 family.,similarity:Contains 1 GAT domain.,similarity:Contains 1 VHS domain.,subunit:Interacts with FYN, GRB2 and PIK3R1 when phosphorylated.,

TM209抗体应用：WB 1:500-2000

TM210抗体应用：WB 1:500-2000

TM217 抗体应用：WB 1:500-2000