Browse our anti-TRPS1 (TRPS1) Antibodies

Full name:
anti-Trichorhinophalangeal Syndrome I Antibodies (TRPS1)
On www.antibodies-online.com are 22 Trichorhinophalangeal Syndrome I (TRPS1) Antibodies from 9 different suppliers available. Additionally we are shipping and many more products for this protein. A total of 26 TRPS1 products are currently listed.
Synonyms:
AI115454, AI447310, D15Ertd586e, GC79, LGCR
list all antibodies Gene Name GeneID UniProt
TRPS1 299897  
TRPS1 7227 Q9UHF7
TRPS1 83925  

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Top referenced anti-TRPS1 Antibodies

  1. Human Polyclonal TRPS1 Primary Antibody for IHC, ELISA - ABIN1534176 : Olsen, Blagoev, Gnad, Macek, Kumar, Mortensen, Mann: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. in Cell 2006 (PubMed)

More Antibodies against TRPS1 Interaction Partners

Human Trichorhinophalangeal Syndrome I (TRPS1) interaction partners

  1. in this kindred support the previous genotype-phenotype results suggesting that patients with more pronounced facial characteristics and more severe shortening of hands and feet are more likely to have mutation in exon 6 of TRPS1

  2. Down-regulation of TRPS1 by miR (show MLXIP Antibodies)-373, acting as a transcriptional activator, promotes epithelial-mesenchymal transition (EMT (show ITK Antibodies)) and metastasis by repressing FOXA1 (show FOXA1 Antibodies) transcription, expanding upon its previously reported role as a transcription repressor.

  3. TRPS1 gene was responsible for most of the TRPS phenotype

  4. Data show that co-silencing of tricho-rhino-phalangeal-syndrome (TRPS1) and cathepsin D (show CTSD Antibodies) (Cath-D) in breast cancer cells (BCC) affects the transcription of cell cycle and proliferation.

  5. Trps1 plays a crucial role in osteosarcoma angiogenesis, metastasis and clinical surgical stage.

  6. Single nucleotide polymorphisms in TRPS1 gene is associated with Coronary Artery Disease.

  7. Missense mutations are located exclusively in exon 6 and 7 of TRPS1 in patients with tricho-rhino-phalangeal syndrome.

  8. TRPS1 haploinsufficiency results in STAT3 (show STAT3 Antibodies) and SOX9 (show SOX9 Antibodies) mRNA expression in Trichorhinophalangeal syndrome.

  9. Trps1 is involved in non-anastomotic biliary structure pathogenesis following liver transplantation and negatively correlates with biliary epithelial cell epithelial-mesenchymal transition and biliary fibrosis in liver grafts.

  10. our study proposes that TRPS1 acts as a central hub in the control of cell cycle and proliferation during cancer development

Mouse (Murine) Trichorhinophalangeal Syndrome I (TRPS1) interaction partners

  1. our findings partially explain why patients with TRPS show a broad range of congenital cardiac defects, although Trps1 expression is observed in a more restricted fashion.

  2. Taken together, these results show that hair follicle development in Trps1 KO embryos is impaired directly or indirectly by decreased Noggin (show NOG Antibodies) expression.

  3. association between SNP within TRPS1 and BMD (show BEST1 Antibodies)

  4. Trps1 acts as a regulator of hdac1 (show HDAC1 Antibodies) and hdac4 (show HDAC5 Antibodies) histone deacetylases during mitosis.

  5. The loss of Trps1 suppresses ureteric bud branching because of the activation of TGF-beta (show TGFB1 Antibodies) signaling.

  6. We found that Trps1 directly represses expression of the hair follicle stem cell regulator Sox9 (show SOX9 Antibodies) to control proliferation of the follicle epithelium.

  7. Trps1 is identified as a potent inhibitor of Dspp (show DSPP Antibodies) expression and the subsequent mineralization of dentin.

  8. analysis of control of mesenchymal lineage progression by microRNAs targeting skeletal gene regulators Trps1 and Runx2 (show RUNX2 Antibodies)

  9. These observations underscore the indispensable role played by Trps1 in normal temporomandibular joint development.

  10. Genetic variation in TRPS1 may regulate hip geometry as well as bone mineral density

TRPS1 Antigen Profile

Antigen Summary

This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III.

Alternative names and synonyms associated with TRPS1

  • trichorhinophalangeal syndrome I (Trps1) antibody
  • trichorhinophalangeal syndrome I (TRPS1) antibody
  • trichorhinophalangeal syndrome I (trps1) antibody
  • trichorhinophalangeal syndrome I (human) (Trps1) antibody
  • AI115454 antibody
  • AI447310 antibody
  • D15Ertd586e antibody
  • GC79 antibody
  • LGCR antibody

Protein level used designations for TRPS1

trichorhinophalangeal syndrome I homolog , zinc finger transcription factor Trps1 , tricho-rhino-phalangeal syndrome type I protein , zinc finger protein GC79 , atypical GATA protein TRPS1

GENE ID SPECIES
299897 Rattus norvegicus
7227 Homo sapiens
399173 Xenopus laevis
83925 Mus musculus
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