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TAPT1 Antibody (C-term) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | Q6NXT6 |
|---|---|
| Clone Names | 91208335 |
| Gene ID | 202018 |
|---|---|
| Other Names | Transmembrane anterior posterior transformation protein 1 homolog, Cytomegalovirus partial fusion receptor, TAPT1, CMVFR |
| Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
| Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
| Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
| Name | TAPT1 |
|---|---|
| Synonyms | CMVFR |
| Function | Plays a role in primary cilia formation (PubMed:26365339). May act as a downstream effector of HOXC8 possibly by transducing or transmitting extracellular information required for axial skeletal patterning during development (By similarity). May be involved in cartilage and bone development (By similarity). May play a role in the differentiation of cranial neural crest cells (By similarity). |
| Cellular Location | Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton, cilium basal body. Membrane; Multi-pass membrane protein |
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes a highly conserved, putativetransmembrane protein. A mutation in the mouse ortholog of thisgene results in homeotic, posterior-to-anterior transformations ofthe axial skeleton which are similar to the phenotype of mousehomeobox C8 gene mutants. This gene is proposed to functiondownstream of homeobox C8 to transduce extracellular patterninginformation during axial skeleton development. An alternativelyspliced transcript variant encoding a substantially differentisoform has been described, but its biological validity has notbeen determined.
References
Howell, G.R., et al. Genetics 175(2):699-707(2007)Baldwin, B.R., et al. J. Gen. Virol. 81 (PT 1), 27-35 (2000) :Baldwin, B.R., et al. Biochem. Biophys. Res. Commun. 219(2):668-673(1996)
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