FLCN (NM_144606) Human Untagged Clone

CAT#: SC123173

FLCN (untagged)-Human folliculin (FLCN), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: FLCN
• Synonyms: BHD; DENND8B; FLCL
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_144606 edited
  GGTCGCTCCTGGTTCTGCCAGCTCCCCTGAGAGCCTGAACCCGGGCTTGAGAGCCTCGCC
  ACCCCGGGTGACATCCCTGCCGTGGGCTTGGGGGCTCTGGGTGTGATTCCGCCGGTCCGG
  GTCCCGCAGCGACCACCTACCCAGCGCAGTCAGGGGTGGGGCTGGGACCCAGAGCGGGAC
  CCCGGCTGCCGAGTCCAGGTGTCCCGCGGGCCTCGATTTGGGGAGCAGAAAACGCCAGGT
  CTTCAAGGGTGTCTGCCACCACCATGCCTGACCCATTTGGCAGCAGCCTCGTGTGTGGTG
  GTCTGGTGTGGACGGTGGAAGCGTGATTCTGCTGAGTGTCAGTGTGACCACTCGTGCTCA
  GCCGTATCTCAGCAGGAGGACAGGTGCCGGAGCAGCTCGTGCAGCTAAGCAGCCAACTGC
  AGAAACGTCAGGCCTGTTGCAGTCTCCAAGGCACCATGAATGCCATCGTGGCTCTCTGCC
  ACTTCTGCGAGCTCCACGGCCCCCGCACTCTCTTCTGCACGGAGGTGCTGCACGCCCCAC
  TTCCTCAAGGGGATGGGAATGAGGACAGTCCTGGCCAGGGTGAGCAGGCGGAAGAAGAGG
  AAGGTGGCATTCAGATGAACAGTCGGATGCGTGCGCACAGCCCCGCAGAGGGGGCCAGCG
  TCGAGTCCAGCAGCCCGGGGCCCAAAAAGTCGGACATGTGCGAGGGCTGCCGGTCACTTG
  CTGCAGGGCACCCGGGATATATCAGCCATGATAAAGAGACCTCCATTAAATACGTCAGCC
  ACCAGCACCCCAGCCACCCCCAGCTCTTCAGCATTGTCCGCCAGGCCTGTGTCCGGAGCC
  TGAGCTGTGAGGTCTGCCCTGGCCGTGAAGGCCCCATCTTCTTCGGAGATGAGCAGCACG
  GCTTTGTGTTCAGCCACACCTTCTTCATCAAGGACAGCCTGGCCAGGGGCTTCCAGCGCT
  GGTACAGCATCATCACCATCATGATGGACCGGATCTACCTCATCAACTCCTGGCCCTTCC
  TGCTGGGGAAGGTCCGGGGAATCATCGATGAGCTCCAGGGCAAGGCGCTCAAGGTGTTTG
  AGGCAGAGCAGTTTGGATGCCCACAGCGTGCTCAGAGGATGAACACAGCCTTCACGCCAT
  TCCTACACCAGAGGAACGGCAACGCCGCCCGCTCGCTGACATCGCTGACAAGTGATGACA
  ACCTGTGGGCGTGCCTGCACACCTCCTTTGCCTGGCTCCTGAAGGCGTGTGGCAGCCGGC
  TGACCGAGAAGCTCCTGGAAGGTGCTCCGACCGAGGATACCTTGGTCCAGATGGAGAAGC
  TCGCTGGTGAGGCAGGGGTGCTGTTGCCGGGGCCTTGGCCCGGATGGCCGTGGGGCGGTA
  CCAGCTGTCTGCTCTCCTGGCAGGAATCGCTGAGGGAGGGAAACGCGGCTCTGAATCAGC
  CCAGAACGAGCCTTCGGGAAGCTCACCCTCCGATCTCGGTGTGATTGTTGTGATTGTTGT
  GATTTCCTGTCTCGTTTGCCTTGACCGCCATGTGAAAGAATCTGTTCCCCAGCTAGGTGG
  GGAAAATTCACAGGTGGGCTGTCTGTAGAGAGAACTGGCTGATTAAAGGCTTCTCGTCCC
  GATTTTGTGATAGCCAAGTGCTTGGCCTGGTCGACGGTCTTTGCTCCTTTACAAATAAAG
  TGTTCTGTTTCAAAAAAAAAAAAAAAAAAAA
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_144606 unedited
  NGCCTTCGCATTTGTATACGACTTATATAGGCGGCCCGATTCGCACGAGGGTCGCTCCTG
  GTTCTGCCAGCTCCCCTGANAGCCTGAACCCGGGCTTGAGAGCCTCGCCACCCCGGGTGA
  CATCCCTGCCGTGGGCTTGGGGGCTCTGGGTGTGATTCCGCCGGTCCGGGTCCCGCAGCG
  ACCACCTACCCAGCGCAGTCAGGGGTGGGGCTGGGACCCAGAGCGGGACCCCGGCTGCCG
  AGTCCAGGTGTCCCGCGGGCCTCGATTTGGGGAGCAGAAAACGCCAGGTCTTCAAGGGTG
  TCTGCCACCACCATGCCTGACCCATTTGGCAGCAGCCTCGTGTGTGGTGGTCTGGTGTGG
  ACGGTGGAAGCGTGATTCTGCTGAGTGTCAGTGTGACCACTCGTGCTCAGCCGTATCTCA
  GCAGGAGGACAGGTGCCGGAGCAGCTCGTGCAGCTAAGCAGCCAACTGCAGAAACGTCAG
  GCCTGTTGCAGTCTCCAAGGCACCATGAATGCCATCGTGGCTCTCTGCCACTTCTGCGAG
  CTCCACGGCCCCCGCACTCTCTTCTGCACGGAGGTGCTGCACGCCCCACTTCCTCAAGGG
  GATGGGAATGAGGACAGTCCTGGCCAGGGTGAGCAGGCGGAAGAAGAGGAAGGTGGCATT
  CAGATGAACAGTCGGATGCGTGCGCACAGCCCCGCAGAGGGGGCCAGCGTCGAGTCCAGC
  AGCCCGGGGCCCATAAGTCNGACATGTGCGATGGCTGCCGGTCACTTGCTGCAGGGCACC
  CGGGATATATCAGCCATGATAAAGAGACCTCCATTAAATACGTCAGCCACCAGCACCCCA
  GCCACCCCCAGCTCTTCAGCATTGTCCGCCAGGCCTGTGTCCAGAGCCTGG
  
• Restriction Sites: Please inquire
• ACCN: NM_144606
• ORF Size: 1029 bp
• Insert Size: 1720
• 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_144606.4, NP_653207.1
• RefSeq Size: 1754
• RefSeq ORF: 1029
• Locus ID: 201163
• Protein Families: Druggable Genome
• Protein Pathways: Renal cell carcinoma
• Gene Summary: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
  Transcript Variant: This variant (2) uses an alternate splice site in the 3' coding region, as compared to variant 1. Isoform 2 has a shorter and distinct C-terminus, as compared to isoform 1.