TLX1抗体应用：WB 1:500-2000 ELISA 1:5000-20000T-cell leukemia homeobox 1(TLX1) Homo sapiens This gene encodes a nuclear transcription factor that belongs to the NK-linked or NK-like (NKL) subfamily of homeobox genes. The encoded protein is required for normal development of the spleen during embryogenesis. This protein is also involved in specification of neuronal cell fates. Ectopic expression of this gene due to chromosomal translocations is associated with certain T-cell acute lymphoblastic leukemias. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010],

TLX2抗体应用：WB 1:500-2000This gene is a member of an orphan homeobox-containing transcription factor family. Studies of the mouse ortholog have shown that the encoded protein is crucial for the development of the enteric nervous system; in humans, loss-of-function may play a role in tumorigenesis of gastrointestinal stromal tumors. [provided by RefSeq, May 2010],

TLX3抗体应用：WB 1:500-2000 ELISA 1:5000-20000T-cell leukemia homeobox 3(TLX3) Homo sapiens The protein encoded by this gene is an orphan homeobox protein that encodes a DNA-binding nuclear transcription factor. A translocation [t(5;14)(q35;q32)] involving this gene is associated with T-cell acute lymphoblastic leukemia (T-ALL) in children and young adults. [provided by RefSeq, Nov 2015],

TM100抗体应用：WB 1:500-2000

TM11D抗体应用：WB 1:500-2000 ELISA 1:5000-20000transmembrane protease, serine 11D(TMPRSS11D) Homo sapiens This gene encodes a trypsin-like serine protease released from the submucosal serous glands onto mucous membrane. It is a type II integral membrane protein and has 29-38% identity in the sequence of the catalytic region with human hepsin, enteropeptidase, acrosin, and mast cell tryptase. The noncatalytic region has little similarity to other known proteins. This protein may play some biological role in the host defense system on the mucous membrane independently of or in cooperation with other substances in airway mucous or bronchial secretions. [provided by RefSeq, Jul 2008],

TM136抗体应用：WB 1:500-2000

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