TAPT1 (NM_153365) Human Untagged Clone

CAT#: SC317972

TAPT1 (untagged)-Human transmembrane anterior posterior transformation 1 (TAPT1)

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: TAPT1
• Synonyms: CMVFR; OCLSBG
• Vector: pCMV6-XL4
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_153365 edited
  ATGGCGGGCGTCGGCGACGCGGCCGCTCCGGGAGAAGGCGGCGGTGGCGGCGTGGACGGC
  CCGCAGCGGGACGGCCGCGGCGAGGCGGAGCAGCCGGGCGGCAGCGGCGGACAGGGGCCC
  CCGCCGGCGCCTCAGCTCACAGAGACGCTGGGCTTCTACGAGAGCGACCGGCGGCGGGAG
  AGGCGCCGGGGCCGCACAGAGCTTTCATTGTTGAGGTTCCTCAGTGCTGAACTAACAAGA
  GGGTACTTCCTTGAACATAATGAGGCCAAGTATACAGAAAGAAGAGAAAGAGTATACACT
  TGTTTGCGAATACCAAGAGAATTGGAAAAGCTGATGGTTTTTGGAATCTTTCTGTGCCTG
  GATGCGTTTTTGTATGTGTTCACCCTGCTTCCTTTAAGAGTTTTCCTGGCACTATTCAGG
  CTCCTCACTTTGCCTTGCTATGGCTTAAGGGACAGACGTTTGCTTCAGCCTGCCCAGGTG
  TGTGACATTTTGAAGGGTGTCATTTTGGTAATCTGCTATTTTATGATGCACTATGTTGAC
  TACTCCATGATGTACCACCTGATAAGGGGGCAGTCCGTCATCAAGCTCTACATCATCTAC
  AACATGCTGGAGGTAGCTGATCGTCTGTTTTCATCTTTTGGACAAGACATATTAGATGCT
  CTCTATTGGACAGCAACAGAGCCTAAAGAAAGAAAAAGAGCCCACATTGGGGTGATTCCT
  CACTTTTTCATGGCTGTTCTCTATGTCTTTTTGCATGCAATTCTTATAATGGTTCAAGCA
  ACAACTCTCAATGTAGCTTTTAACTCACACAACAAGTCTTTGCTTACTATCATGATGTCT
  AATAATTTTGTTGAAATTAAAGGAAGTGTTTTCAAGAAGTTTGAAAAGAACAATCTCTTT
  CAAATGTCAAATAGCGATATTAAGGAACGATTCACAAATTATGTGCTTTTACTGATAGTG
  TGTCTAAGAAACATGGAACAGTTTTCTTGGAATCCAGATCATCTCTGGGTGTTGTTTCCA
  GATGTCTGTATGGTAATTGCATCAGAAATTGCCGTGGATATTGTAAAACATGCCTTTATT
  ACTAAATTCAATGACATTACTGCAGATGTCTACAGTGAATATAGAGCCAGTCTTGCTTTT
  GACCTTGTTAGCAGCCGACAGAAAAATGCATACACTGATTACAGTGACTCTGTAGCACGG
  AGGATGGGCTTTATTCCTCTCCCACTAGCTGTTTTACTCATCAGAGTTGTAACAAGCTCA
  ATTAAAGTGCAAGGAATCCTGTCTTATGCCTGTGTCATACTCTTCTATTTTGGGTTGATA
  TCCCTGAAAGTACTTAATAGCATCGTGCTGTTGGGGAAATCGTGCCAGTATGTGAAGGAA
  GCCAAAATGGAAGAGAAGCTGTCGAATCCTCCCGCAACCTGCACTCCAGGCAAGCCGTCC
  AGTAAATCACAGAACAAATGTAAACCCTCTCAAGGCCTTTCCACAGAAGAAAACCTGTCT
  GCCTCCATCACCAAACAACCTATTCATCAAAAGGAAAATATCATACCATTACTTGTGACA
  AGCAATTCTGATCAGTTTTTGACAACTCCAGATGGTGACGAGAAGGACATAACGCAGGAC
  AATTCTGAATTAAAACACAGATCCTCAAAGAAAGATTTGTTAGAGATAGACAGGTTCACA
  ATTTGTGGAAACCGAATTGACTGA
  
• Restriction Sites: Please inquire
• ACCN: NM_153365
• ORF Size: 1704 bp
• Insert Size: 1700
• OTI Disclaimer: Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery.
  
  The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
• OTI Annotation: This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.

Reference Data

• RefSeq: NM_153365.2, NP_699196.2
• RefSeq Size: 4610
• RefSeq ORF: 1704
• Locus ID: 202018
• Domains: DUF747
• Protein Families: Druggable Genome, Transmembrane
• Gene Summary: This gene encodes a highly conserved protein that localizes to the centrosome and/or ciliary basal body. Mutations in this gene disrupt Golgi morphology and trafficking and normal primary cilium formation and these mutations are congenitally manifested by severe undermineralization of the intra-uterine skeleton. A mutation in the mouse ortholog of this gene results in homeotic, posterior-to-anterior transformations of the axial skeleton which are similar to the phenotype of mouse homeobox C8 gene mutants. In mouse, this gene is thought to function downstream of homeobox C8 to transduce extracellular patterning information during axial skeleton development. [provided by RefSeq, Jan 2017]