Netrin G1 (NTNG1) (NM_014917) Human Untagged Clone

CAT#: SC114761

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


  "NM_014917" in other vectors (5)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol NTNG1
Synonyms Lmnt1
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>NCBI ORF sequence for NM_014917, the custom clone sequence may differ by one or more nucleotides


ATGTATTTGTCAAGATTCCTGTCGATTCATGCCCTTTGGGTTACGGTGTCCTCAGTGATGCAGCCCTACC
CTTTGGTTTGGGGACATTATGATTTGTGTAAGACTCAGATTTACACGGAAGAAGGGAAAGTTTGGGATTA
CATGGCCTGCCAGCCGGAATCCACGGACATGACAAAATATCTGAAAGTGAAACTCGATCCTCCGGATATT
ACCTGTGGAGACCCTCCTGAGACGTTCTGTGCAATGGGCAATCCCTACATGTGCAATAATGAGTGTGATG
CGAGTACCCCTGAGCTGGCACACCCCCCTGAGCTGATGTTTGATTTTGAAGGAAGACATCCCTCCACATT
TTGGCAGTCTGCCACTTGGAAGGAGTATCCCAAGCCTCTCCAGGTTAACATCACTCTGTCTTGGAGCAAA
ACCATTGAGCTAACAGACAACATAGTTATTACCTTTGAATCTGGGCGTCCAGACCAAATGATCCTGGAGA
AGTCTCTCGATTATGGACGAACATGGCAGCCCTATCAGTATTATGCCACAGACTGCTTAGATGCTTTTCA
CATGGATCCTAAATCCGTGAAGGATTTATCACAGCATACGGTCTTAGAAATCATTTGCACAGAAGAGTAC
TCAACAGGGTATACAACAAATAGCAAAATAATCCACTTTGAAATCAAAGACAGGTTCGCGTTTTTTGCTG
GACCTCGCCTACGCAATATGGCTTCCCTCTACGGACAGCTGGATACAACCAAGAAACTCAGAGATTTCTT
TACAGTCACAGACCTGAGGATAAGGCTGTTAAGACCAGCCGTTGGGGAAATATTTGTAGATGAGCTACAC
TTGGCACGCTACTTTTACGCGATCTCAGACATAAAGGTGCGAGGAAGGTGCAAGTGTAATCTCCATGCCA
CTGTATGTGTGTATGACAACAGCAAATTGACATGCGAATGTGAGCACAACACTACAGGTCCAGACTGTGG
GAAATGCAAGAAGAATTATCAGGGCCGACCTTGGAGTCCAGGCTCCTATCTCCCCATCCCCAAAGGCACT
GCAAATACCTGTATCCCCAGTATTTCCAGTATTGGTACGAATGTCTGCGACAACGAGCTCCTGCACTGCC
AGAACGGAGGGACGTGCCACAACAACGTGCGCTGCCTGTGCCCGGCCGCATACACGGGCATCCTCTGCGA
GAAGCTGCGGTGCGAGGAGGCTGGCAGCTGCGGCTCCGACTCTGGCCAGGGCGCGCCCCCGCACGGCTCC
CCAGCGCTGCTGCTGCTGACCACGCTGCTGGGAACCGCCAGCCCCCTGGTGTTCTAG


>OriGene 5' read for NM_014917 unedited
NGGGTCAAATTTGTATACGACTCATATAGGCGGCCGCGNAATTCGCACGAGGCTCCGAGA
GGGGGCGACTTGCAGGAGGCTCCCCCCGGGGGCGGAGGCGAAGGGTGTTGGTGCCAGAAG
AAAAGAATGATTGATGGGAAACAGACACCGGGCTATAGACACTCATCCTTTTGCTTCAGA
TACTGATATCTCAGCCTGCTTGAGCATCCCTTGTGAGCTGTGAACATTGAGGATCACTCA
GGGTTATCGGATGTACAACGGGAGAGCCATCGCTTTGCTAAATTATTATCTGCAATTGGA
CATCTTTTACAAAAACCAAACTAGACCTGAGTCTAATAGATATGTTCTAAGACAAAGAAA
AAGCTGCAAGTTGTTAACGCCTAACACACAAGTATGTTAGGCTTCCACCAAAGTCCTCAA
TATACCTGAATACGCACAATATCTTAACTCTTCATATTTGGTTTTGGGATCTGCTTTGAG
GTCCCATCTTCATTTAAAAAAAAATACAGAGACCTACCTACCCGTACGCATACATACATA
TGTGTATATATATGTAAACTAGACAAAGATCGCAGATCATAAAGCAAGCTCTGCTTTAGT
TTCCAAGAAGATTACAAAGAATTTAGAGATGTATTTGTCAAGATTCCTGTCGATTCATGC
CCTTTGGGTTACGGTGTCCTCAGTGATGCAGCCCTACCCTTTGGTTTGGGGACATTATGA
TTTGTGTAAGACTCAGATTTACACGGAAGAAGGGGAAGTTTGGGATTACATGGCCTGCCA
GCCGGNAATCCACGGACATGACAAAATCTGAAAGTGAAACTCGATCCTCCGGATATTACC
TGTGGAGACCCTNCTGAGACGTTCTGTGCATGGGCATCCNTACTGTGCATAATGAGTGGA
TGCGAGTACCCTGAGCTGCACACCCCCTGAGCTGA
Restriction Sites ECoRI-NOT     
ACCN NM_014917
ORF Size 3015 bp
Insert Size 4110
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_014917.1, NP_055732.1
RefSeq Size 3015
RefSeq ORF 3015
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.

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