ENAH (NM_018212) Human Untagged Clone

CAT#: SC317978

ENAH (untagged)-Human enabled homolog (Drosophila) (ENAH), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: ENAH
• Synonyms: ENA; MENA; NDPP1
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_018212, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGAGTGAACAGAGTATCTGTCAGGCAAGAGCTGCTGTGATGGTTTATGATGATGCCAATAAGAAGTGGG
  TGCCAGCTGGTGGCTCAACTGGATTCAGCAGAGTTCATATCTATCACCATACAGGCAACAACACATTCAG
  AGTGGTGGGCAGGAAGATTCAGGACCATCAGGTCGTGATAAACTGTGCCATTCCTAAAGGGTTGAAGTAC
  AATCAAGCTACACAGACCTTCCACCAGTGGCGAGATGCTAGACAGGTGTATGGTCTCAACTTTGGCAGCA
  AAGAGGATGCCAATGTCTTCGCAAGTGCCATGATGCATGCCTTAGAAGTGTTAAATTCACAGGAAACAGG
  GCCAACATTGCCTAGACAAAACTCACAACTACCTGCTCAAGTTCAAAATGGCCCATCCCAAGAAGAATTG
  GAAATTCAAAGAAGACAACTACAAGAACAGCAACGGCAAAAGGAGCTGGAGCGGGAAAGGCTGGAGCGAG
  AAAGAATGGAAAGAGAAAGGTTGGAGAGAGAGAGGTTAGAAAGGGAAAGGCTGGAGAGGGAGCGACTGGA
  ACAAGAACAGCTGGAGAGAGAGAGACAAGAACGGGAACGGCAGGAACGCCTGGAGCGGCAGGAACGCCTG
  GAGCGGCAGGAACGCCTGGAGCGGCAGGAACGCCTGGATCGGGAGAGGCAAGAAAGACAAGAACGAGAGA
  GGCTGGAGAGACTGGAACGGGAGAGGCAAGAAAGGGAGCGACAAGAGCAGTTAGAAAGGGAACAGCTGGA
  ATGGGAGAGAGAGCGCAGAATATCAAGTGCTGCTGCCCCTGCCTCTGTTGAGACTCCTCTAAACTCTGTG
  CTGGGAGACTCTTCTGCTTCTGAGCCAGGCTTGCAGGCAGCCTCTCAGCCGGCCGAGACTCCATCCCAAC
  AGGGCATTGTCTTGGGACCACTTGCACCTCCACCTCCTCCACCACTCCCACCAGGGCCTGCACAGGCTTC
  AGTAGCCCTCCCTCCTCCCCCAGGGCCCCCTCCACCTCCTCCACTCCCATCCACCGGGCCTCCACCGCCC
  CCTCCTCCCCCTCCTCTCCCTAATCAAGTACCCCCTCCTCCTCCACCACCTCCTGCCCCACCCCTCCCTG
  CATCTGGATTCTTTTTGGCATCCATGTCAGAAGACAATCGCCCTTTAACTGGACTTGCAGCTGCAATTGC
  CGGAGCAAAACTTAGGAAAGTGTCACGGATGGAGGATACCTCTTTCCCAAGTGGAGGGAATGCTATTGGT
  GTGAACTCCGCCTCATCTAAAACAGATACAGGCCGTGGAAATGGACCCCTTCCTTTAGGGGGTAGTGGTT
  TAATGGAAGAAATGAGTGCCCTGCTGGCCAGGAGGAGAAGAATTGCTGAAAAGGGATCAACAATAGAAAC
  AGAACAAAAAGAGGACAAAGGTGAAGATTCAGAGCCTGTAACTTCTAAGGCCTCTTCAACAAGTACACCT
  GAACCAACAAGAAAACCTTGGGAAAGAACAAATACAATGAATGGCAGCAAGTCACCTGTTATCTCCAGAC
  CAAAATCCACACCCTTATCACAGCCCAGTGCCAATGGAGTCCAGACGGAAGGACTTGACTATGACAGGCT
  GAAGCAGGACATTTTAGATGAAATGAGAAAAGAATTAACAAAGCTAAAAGAAGAGCTCATTGATGCAATC
  AGGCAGGAACTGAGCAAGTCAAATACTGCATAG
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_018212
• ORF Size: 1713 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_018212.4, NP_060682.2
• RefSeq Size: 13109
• RefSeq ORF: 1713
• Locus ID: 55740
• Protein Pathways: Regulation of actin cytoskeleton
• Gene Summary: This gene encodes a member of the enabled/ vasodilator-stimulated phosphoprotein. Members of this gene family are involved in actin-based motility. This protein is involved in regulating the assembly of actin filaments and modulates cell adhesion and motility. Alternate splice variants of this gene have been correlated with tumor invasiveness in certain tissues and these variants may serve as prognostic markers. A pseudogene of this gene is found on chromosome 3. [provided by RefSeq, Sep 2016]
  Transcript Variant: This variant (2) lacks an alternate in-frame exon compared to variant 1. The resulting isoform (b) has the same N- and C-termini but is shorter compared to 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.