FMN1 (NM_001277313) Human Untagged Clone

CAT#: SC338028

FMN1 (untagged) - Human formin 1 (FMN1), transcript variant 1

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: FMN1
• Synonyms: FMN; LD
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001277313, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGGAAGGCACTCATTGTACCCTCCAATTGCATAAGCCCATTACGGAACTCTGCTACATCAGCTTCTGTC
  TTCCAAAGGGGGAAGTCAGAGGATTTTCATACAAGGGCACTGTAACTCTAGACAGATCCAATAAAGGTTT
  TCATAACTGCTACCAAGTCAGGGAGGAGTCAGACATCATCAGCCTCAGCCAGGAGCCGGACGAACATCCA
  GGCGACATATTTTTCAAGCAGACTCCCACGAAAGACATTCTAACTGAGCTGTACAAACTCACAACAGAGA
  GGGAGAGACTGCTAACCAATCTCCTGAGCTCAGACCACATCCTGGGGATCACGATGGGGAACCAGGAGGG
  GAAGCTGCAAGAGCTGTCCGTGAGCCTGGCCCCCGAGGATGACTGTTTCCAGAGTGCTGGTGACTGGCAG
  GGAGAGCTCCCCGTGGGCCCTCTCAATAAGAGGAGCACCCACGGGAACAAAAAGCCTCGGAGGTCTAGTG
  GAAGGAGAGAGAGCTTTGGGGCCCTTCCACAGAAGAGGACCAAAAGAAAAGGGCGTGGAGGCCGAGAATC
  AGCTCCTCTGATGGGCAAGGACAAGATCTGTTCCAGCCACTCCCTTCCTCTTTCTAGAACAAGGCCTAAC
  CTTTGGGTACTAGAGGAGAAAGGAAATCTGCTCCCGAATGGGGCACTTGCCTGCTCCCTGCAGAGGAGAG
  AGAGCTGCCCCCCAGATATTCCCAAGACGCCAGACACAGACCTTGGCTTTGGGAGCTTTGAGACGGCTTT
  CAAGGACACTGGGCTTGGAAGAGAAGTGCTGCCCCCTGACTGCAGCTCCACAGAGGCAGGAGGGGATGGC
  ATTCGGAGGCCGCCGAGCGGGCTGGAGCATCAGCAAACAGGTTTGTCTGAAAGTCACCAGGACCCTGAGA
  AGCATCCAGAGGCAGAAAAGGATGAGATGGAGAAGCCGGCTAAGCGGACTTGCAAGCAGAAACCTGTCTC
  CAAAGTGGTGGCCAAAGTTCAGGACCTGTCCTCCCAGGTACAAAGAGTAGTTAAAACGCATTCTAAGGGT
  AAGGAGACGATTGCCATTCGCCCAGCAGCCCACGCTGAGTTTGTACCCAAAGCCGACTTGCTCACCCTCC
  CGGGAGCTGAGGCTGGGGCTCATGGCTCCAGGCGGCAGGGCAAGGAGCGGCAAGGGGATAGGTCATCGCA
  GTCGCCAGCCGGGGAAACAGCCTCCATTTCTAGTGTGTCGGCCAGTGCCGAGGGGGCCGTGAACAAGGTC
  CCCCTGAAGGTGATAGAGAGTGAGAAGTTAGATGAAGCCCCTGAGGGGAAAAGACTGGGCTTCCCTGTCC
  ACACGAGTGTCCCTCACACTCGCCCAGAAACGAGAAACAAGAGGAGAGCCGGGTTGCCCCTTGGTGGCCA
  CAAGTCCTTGTTTCTGGATCTGCCCCACAAAGTAGGTCCTGACTCCTCACAACCCAGAGGTGATAAGAAG
  AAGCCATCCCCACCAGCACCGGCAGCTCTTGGCAAGGTGTTTAATAATTCAGCCTCGCAGTCCAGCACAC
  ACAAACAGACGTCACCTGTTCCCTCGCCTCTGTCTCCAAGGCTCCCCAGCCCTCAGCAGCATCACAGGAT
  CCTCCGGCTCCCTGCATTGCCTGGTGAGAGGGAAGCTGCTCTTAATGACTCTCCTTGTAGAAAGAGCCGT
  GTCTTCTCTGGGTGCGTCTCTGCTGACACCTTGGAGCCACCATCCTCTGCAAAGGTCACGGAGACCAAAG
  GAGCCAGCCCGGCCTTCCTCAGAGCAGGCCAACCTCGGTTGGTGCCTGGGGAAACTTTGGAAAAGAGCTT
  GGGGCCAGGGAAGACCACAGCTGAGCCCCAGCACCAGTCACCTCCAGGTATCTCCTCTGAGGGCTTTCCC
  TGGGACGGCTTCAATGAGCAGACACCTAAAGACCTTCCCAACAGAGATGGAGGCGCGTGGGTTCTGGGCT
  ACAGAGCGGGACCAGCCTGTCCATTTTTGCTTCATGAGGAAAGGGAGAAGTCAAACAGGAGCGAATTGTA
  CTTGGATCTCCATCCTGACCACAGCCTGACTGAGCAGGATGACAGGACTCCTGGCAGACTTCAAGCTGTC
  TGGCCACCCCCAAAGACAAAAGACACAGAAGAAAAAGTGGGACTGAAGTACACTGAAGCAGAATACCAAG
  CTGCTATTTTACACTTGAAGAGGGAGCACAAAGAAGAAATTGAAAACCTGCAGGCACAGTTTGAACTTCG
  GGCATTTCATATCCGGGGCGAGCATGCAATGATAACAGCGAGACTAGAAGAAACCATTGAAAATCTGAAA
  CACGAGCTAGAACACAGATGGCGAGGGGGTTGTGAAGAGAGGAAAGATGTGTGCATTTCCACCGATGATG
  ACTGCCCTCCAAAGACCTTCAGAAATGTGTGCGTCCAGACAGACAGAGAGACCTTCCTCAAGCCCTGTGA
  AAGTGAAAGCAAGACAACCAGAAGTAATCAATTAGTACCCAAAAAGCTGAATATCTCCTCTTTAAGCCAG
  CTCTCACCCCCAAATGACCACAAAGACATCCATGCAGCACTCCAGCCAATGGAGGGCATGGCATCAAATC
  AGCAGAAGGCATTGCCTCCGCCTCCCGCATCCATCCCTCCCCCTCCGCCCCTCCCCTCAGGACTTGGATC
  TTTGTCTCCCGCACCTCCAATGCCACCTGTGAGTGCTGGGCCACCGCTACCACCTCCGCCTCCTCCACCG
  CCACCTCTACCTCCACCTTCAAGTGCTGGACCTCCACCACCCCCACCCCCACCCCCACTTCCTAACTCCC
  CTGCCCCACCCAACCCTGGAGGGCCTCCTCCTGCTCCACCACCCCCAGGACTTGCACCCCCACCTCCCCC
  TGGACTCTTCTTTGGACTTGGCTCTTCTTCCAGTCAATGTCCTCGAAAACCAGCCATCGAGCCCAGTTGT
  CCCATGAAGCCTTTATATTGGACTAGGATACAAATAAGTGATAGGAGCCAAAATGCTACACCAACCTTAT
  GGGACTCCTTAGAAGAACCTGACATTCGGGACCCCAGTGAATTTGAGTATTTATTCTCCAAAGACACAAC
  TCAACAGAAGAAAAAACCTCTGTCAGAGACTTATGAGAAGAAAAACAAGGTCAAAAAGATCATCAAATTG
  TTGGATGGAAAACGATCTCAAACTGTGGGAATCTTGATATCTAGTTTACATTTAGAAATGAAGGATATCC
  AACAGGCCATTTTCAATGTGGATGACTCCGTGGTTGATCTGGAGACCCTGGCAGCCTTATATGAAAACAG
  AGCCCAAGAGGATGAGCTGGTTAAAATAAGAAAGTATTACGAGACATCCAAAGAAGAAGAACTGAAGCTG
  CTGGATAAACCTGAGCAATTTTTACATGAGTTAGCCCAGATTCCTAATTTTGCTGAACGTGCCCAGTGCA
  TAATCTTCAGATCTGTCTTTTCTGAGGGTATCACCTCCTTGCACAGAAAGGTAGAGATCATCACGCGAGC
  TTCTAAGGACTTGCTGCACGTGAAGAGCGTGAAGGATATTTTAGCTCTCATCTTGGCTTTTGGAAATTAT
  ATGAATGGAGGAAATAGGACTCGGGGACAAGCCGATGGATATAGCTTAGAAATTCTGCCCAAACTCAAGG
  ATGTCAAAAGTCGGGATAATGGGATTAATCTGGTGGACTACGTTGTTAAGTATTACCTGCGTTACTATGA
  TCAGGAAGCTGGAACAGAAAAGAGTGTTTTCCCCTTGCCGGAACCACAGGATTTCTTTCTGGCCTCCCAA
  GTCAAGTTTGAAGACCTCATAAAAGATTTGAGAAAACTGAAGAGGCAACTAGAAGCAAGTGAGAAACAGA
  TGGTGGTGGTGTGCAAGGAGTCCCCAAAGGAGTATCTCCAGCCTTTCAAGGACAAACTAGAGGAGTTCTT
  CCAAAAAGCCAAAAAAGAGCATAAGATGGAAGAAAGTCACTTGGAGAATGCACAGAAAAGTTTTGAAACA
  ACAGTACGATATTTTGGGATGAAGCCAAAGTCTGGTGAGAAGGAGATCACACCCAGCTACGTGTTTATGG
  TGTGGTATGAGTTCTGCAGTGACTTCAAGACAATTTGGAAACGGGAGAGTAAAAACATATCTAAAGAAAG
  ATTGAAAATGGCTCAGGAATCAGTCAGCAAGTTGACTTCAGAGAAGAAAGTGGAGACAAAGAAAATCAAT
  CCCACTGCTAGCCTGAAAGAAAGACTGCGTCAGAAGGAAGCCAGTGTGACCACTAACTAA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001277313
• ORF Size: 4260 bp
• OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).

Reference Data

• RefSeq: NM_001277313.1, NP_001264242.1
• RefSeq Size: 13546
• RefSeq ORF: 4260
• Locus ID: 342184
• Gene Summary: This gene belongs to the formin homology family and encodes a protein that has a role in the formation of adherens junction and the polymerization of linear actin cables. The homologous gene in mouse is associated with limb deformity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]
  Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a). The exon combination of this variant is inferred based on partial human and full-length orthologous transcript alignments. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.