Netrin G1 (NTNG1) (NM_014917) Human Untagged Clone

CAT#: SC324248

NTNG1 (untagged)-Human netrin G1 (NTNG1), transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: NTNG1
• Synonyms: Lmnt1
• Vector: pCMV6-AC
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_014917.2 TGCAGCCGGAGCAGCACCAGCAACAGCAACAGCGAGCGGGACGGAGTTAGGACCGCTCGG
  AGCGCACAGGTCTCGAGGGTGTTGGTGCCAGAAGAAAAGAATGATTGATGGGAAACAGAC
  ACCGGGCTATAGACACTCATCCTTTTGCTTCAGATACTGATATCTCAGCCTGCTTGAGCA
  TCCCTTGTGAGCTGTGAACATTGAGGATCACTCAGGGTTATCGGATGTACAACGGGAGAG
  CCATCGCTTTGCTAAATTATTATCTGCAATTGGACATCTTTTACAAAAACCAAACTAGAC
  CTGAGTCTAATAGATATGTTCTAAGACAAAGAAAAAGCTGCAAGTTGTTAACGCCTAACA
  CACAAGTATGTTAGGCTTCCACCAAAGTCCTCAATATACCTGAATACGCACAATATCTTA
  ACTCTTCATATTTGGTTTTGGGATCTGCTTTGAGGTCCCATCTTCATTTAAAAAAAAATA
  CAGAGACCTACCTACCCGTACGCATACATACATATGTGTATATATATGTAAACTAGACAA
  AGATCGCAGATCATAAAGCAAGCTCTGCTTTAGTTTCCAAGAAGATTACAAAGAATTTAG
  AGATGTATTTGTCAAGATTCCTGTCGATTCATGCCCTTTGGGTTACGGTGTCCTCAGTGA
  TGCAGCCCTACCCTTTGGTTTGGGGACATTATGATTTGTGTAAGACTCAGATTTACACGG
  AAGAAGGGAAAGTTTGGGATTACATGGCCTGCCAGCCGGAATCCACGGACATGACAAAAT
  ATCTGAAAGTGAAACTCGATCCTCCGGATATTACCTGTGGAGACCCTCCTGAGACGTTCT
  GTGCAATGGGCAATCCCTACATGTGCAATAATGAGTGTGATGCGAGTACCCCTGAGCTGG
  CACACCCCCCTGAGCTGATGTTTGATTTTGAAGGAAGACATCCCTCCACATTTTGGCAGT
  CTGCCACTTGGAAGGAGTATCCCAAGCCTCTCCAGGTTAACATCACTCTGTCTTGGAGCA
  AAACCATTGAGCTAACAGACAACATAGTTATTACCTTTGAATCTGGGCGTCCAGACCAAA
  TGATCCTGGAGAAGTCTCTCGATTATGGACGAACATGGCAGCCCTATCAGTATTATGCCA
  CAGACTGCTTAGATGCTTTTCACATGGATCCTAAATCCGTGAAGGATTTATCACAGCATA
  CGGTCTTAGAAATCATTTGCACAGAAGAGTACTCAACAGGGTATACAACAAATAGCAAAA
  TAATCCACTTTGAAATCAAAGACAGGTTCGCGTTTTTTGCTGGACCTCGCCTACGCAATA
  TGGCTTCCCTCTACGGACAGCTGGATACAACCAAGAAACTCAGAGATTTCTTTACAGTCA
  CAGACCTGAGGATAAGGCTGTTAAGACCAGCCGTTGGGGAAATATTTGTAGATGAGCTAC
  ACTTGGCACGCTACTTTTACGCGATCTCAGACATAAAGGTGCGAGGAAGGTGCAAGTGTA
  ATCTCCATGCCACTGTATGTGTGTATGACAACAGCAAATTGACATGCGAATGTGAGCACA
  ACACTACAGGTCCAGACTGTGGGAAATGCAAGAAGAATTATCAGGGCCGACCTTGGAGTC
  CAGGCTCCTATCTCCCCATCCCCAAAGGCACTGCAAATACCTGTATCCCCAGTATTTCCA
  GTATTGGTACGAATGTCTGCGACAACGAGCTCCTGCACTGCCAGAACGGAGGGACGTGCC
  ACAACAACGTGCGCTGCCTGTGCCCGGCCGCATACACGGGCATCCTCTGCGAGAAGCTGC
  GGTGCGAGGAGGCTGGCAGCTGCGGCTCCGACTCTGGCCAGGGCGCGCCCCCGCACGGCT
  CCCCAGCGCTGCTGCTGCTGACCACGCTGCTGGGAACCGCCAGCCCCCTGGTGTTCTAGG
  TGTCACCTCCAGCCACACCGGACGGGCCTGTGCCGTGGGGAAGCAGACACAACCCAAACA
  TTTGCTACTAACATAGGAAACACACACATACAGACACCCCCACTCAGACAGTGTACAAAC
  TAAGAAGGCCTAACTGAACTAAGCCATATTTATCACCCGTGGACAGCACATCCGAGTCAA
  GACTGTTAATTTCTGACTCCAGAGGAGTTGGCAGCTGTTGATATTATCACTGCAAATCAC
  ATTGCCAGCTGCAGAGCATATTGTGGATTGGAAAGGCTGCGACAGCCCCCCAAACAGGAA
  AGACAAAAAACAAACAAATCAACCGACCTAAAAACATTGGCTACTCTAGCGTGGTGCGCC
  CTAGTACGACTCCGCCCAGTGTGTGGACCAACCAAATAGCATTCTTTGCTGTCAGGTGCA
  TTGTGGGCATAAGGAAATCTGTTACAAGCTGCCATATTGGCCTGCTTCCGTCCCTGAATC
  CCTTCCAACCTGTGCTTTAGTGAACGTTGCTCTGTAACCCTTGTTGGTTGAAAGATTTCT
  TTGTCTGATGTTAGTGATGCACATGTGTAACAGCCCCCTCTAAAAGCGCAAGCCAGTCAT
  ACCCCTGTATATCTTAGCAGCACTGAGTCCAGTGCGAGCACACACCCACTATACAAGAGT
  GGCTATAGGAAAAAAGAAAGTGTATCTATCCTTTTGTATTCAAATGAAGTTATTTTTCTT
  GAACTACTGTAATATGTAGATTTTTTGTATTATTGCCAATTTGTGTTACCAGACAATCTG
  TTAATGTATCTAATTCGAATCAGCAAAGACTGACATTTTATTTTGTCCTCTTTCGTTCTG
  TTTTGTTTCACTGTGCAGAGATTTCTCTGTAAGGGCAACGAACGTGCTGGCATCAAAGAA
  TATCAGTTTACATATATAACAAGTGTAATAAGATTCCACCAAAGGACATTCTAAATGTTT
  TCTTGTTGCTTTAACACTGGAAGATTTAAAGAATAAAAACTCCTGCATAAACAAAAAAAA
  AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
  AAAAAAAAAAAAAAA
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_014917.2 unedited
  GACATTTTGTATACGACTCCTATAGGGCGGCCGGCGACTCGCGGCGCGCCGGTACCGGTC
  CGGAATTCCCGGGATTGCAGCCGGAGCAGCACCAGCAACAGCAACAGCGAGCGGGACGGA
  GTTAGGACCGCTCGGAGCGCACAGGTCTCGAGGGTGTTGGTGCCAGAAGAAAAGAATGAT
  TGATGGGAAACAGACACCGGGCTATAGACACTCATCCTTTTGCTTCAGATACTGATATCT
  CAGCCTGCTTGAGCATCCCTTGTGAGCTGTGAACATTGAGGATCACTCAGGGTTATCGGA
  TGTACAACGGGAGAGCCATCGCTTTGCTAAATTATTATCTGCAATTGGACTTCTTTTACA
  AAAACCAAACTAGACCTGAGTCTAATAGATATGTTCTAAGACAAAGAAAAAGCTGCAAGT
  TGTTAACGCCTAACACACAAGTATGTTAGGCTTCCACCAAAGTCCTCAATATACCTGAAT
  ACGCACAATATCTTAACTCTTCATATTTGGTTTTGGGATCTGCTTTGAGGTCCCATCTTC
  ATTTAAAAAAAAATACAGAGACCTACCTACCCGTACGCATACATACATATGTGTATATAT
  ATGTAAACTAGACAAAGATCGCAGATCATAAAGCAAGCTCTGCTTTAGTTTCCAAGAAGA
  TTACAAAGAATTTAGAGATGTATTTGTCAAGATTCCTGTCGATTCATGCCCTTTGGGTTA
  CGGTGTCCTCAGTGATGCAGCCCTACCCTTTGGTTTGGGACATTATGATTTGTGTAGACT
  CAGATTTACACGAGAGGAAGTTTGGGATTAACATGGCCTGCCAGCCGATCCACGACATGA
  CAAATATCTGAAGTGAAACTCGATCCTCCGATATTTACCTGTGGAGACCCTCCTGGAGAC
  GTTTCTGTGC
• Restriction Sites: ECoRI-NOT
• ACCN: NM_014917
• ORF Size: 1317 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).
• 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_014917.2, NP_055732.2
• RefSeq Size: 3015
• RefSeq ORF: 1317
• Locus ID: 22854
• Domains: EGF_Lam, laminin_Nterm
• Protein Pathways: Axon guidance
• Gene Summary: This gene encodes a preproprotein that is processed into a secreted protein containing eukaroytic growth factor (EGF)-like domains. This protein acts to guide axon growth during neuronal development. Polymorphisms in this gene may be associated with schizophrenia. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Aug 2015]
  Transcript Variant: This variant (3) contains a longer 5' UTR and lacks two exons in the 3' coding region, but maintains the reading frame, compared to variant 1. The encoded isoform (G1c) is shorter than isoform a. 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.