EYS (NM_001142801) Human Untagged Clone

CAT#: SC326601

EYS (untagged)-Human eyes shut homolog (Drosophila) (EYS), transcript variant 2, mRNA

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: EYS
• Synonyms: bA74E24.1; bA166P24.2; bA307F22.3; C6orf178; C6orf179; C6orf180; dJ22I17.2; dJ303F19.1; dJ1018A4.2; EGFL10; EGFL11; RP25; SPAM
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001142801, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGACTGACAAATCAATCGTCATTCTGAGCCTGATGGTTTTTCACAGCTCTTTCATAAATGGAAAAACAT
  GTAGACGGCAATTGGTGGAAGAATGGCATCCACAACCCTCATCATATGTGGTAAATTGGACACTAACAGA
  AAACATCTGCTTGGACTTCTACAGAGATTGCTGGTTTTTGGGTGTAAACACTAAAATAGATACTTCAGGC
  AATCAAGCTGTTCCCCAGATTTGCCCTTTGCAAATTCAATTAGGAGATATCCTTGTAATTTCTTCTGAAC
  CATCTCTTCAATTTCCAGAAATAAATTTGATGAATGTTTCTGAAACATCTTTCGTTGGCTGTGTGCAAAA
  TACCACAACGGAAGATCAGTTACTTTTTGGCTGCAGACTAAAAGGAATGCACACTGTTAATTCTAAGTGG
  CTGAGTGTTGGGACACATTATTTTATCACAGTTATGGCAAGTGGTCCATCACCTTGTCCACTGGGACTTC
  GACTAAATGTGACAGTGAAACAGCAGTTCTGCCAGGAATCTCTGAGTTCAGAATTTTGCTCTGGTCATGG
  TAAATGTCTTAGTGAAGCTTGGAGCAAGACATATAGCTGCCATTGCCAGCCTCCATTTTCTGGAAAATAC
  TGCCAGGAACTTGATGCATGTTCTTTTAAACCATGTAAAAATAATGGCAGTTGCATTAATAAAAGAGAAA
  ATTGGGATGAGCAAGCATATGAATGTGTCTGTCACCCACCATTTACAGGAAAGAATTGCTCAGAAATAAT
  TGGCCAGTGTCAACCACATGTCTGTTTCCATGGAAACTGCAGCAATATTACTTCAAATAGTTTCATTTGT
  GAATGTGATGAGCAATTTTCAGGTCCATTCTGTGAGGTGTCAGCAAAACCTTGTGTTTCTCTGCTTTTTT
  GGAAAAGAGGAATTTGCCCAAATAGCAGTTCTGCTTATACTTATGAATGCCCAAAAGGATCTTCCAGCCA
  AAATGGTGAAACTGATGTCAGTGAGTTTTCATTAGTACCATGTCAGAATGGTACTGACTGCATCAAAATA
  TCAAATGATGTTATGTGCATCTGTTCACCAATATTTACAGATTTGCTTTGTAAGAGCATTCAAACATCAT
  GTGAGTCATTTCCTTTGAGGAATAATGCTACATGTAAGAAATGTGAGAAAGATTATCCTTGCAGCTGTAT
  ATCAGGATTTACTGAAAAAAACTGTGAGAAAGCAATTGACCACTGTAAACTGCTCAGCATCAACTGTCTG
  AATGAAGAATGGTGTTTCAATATAATTGGAAGATTCAAATATGTATGCATTCCAGGGTGCACAAAAAATC
  CATGTTGGTTTTTGAAGAATGTTTACCTAATTCATCAACACCTCTGCTACTGTGGAGTCACCTTCCATGG
  TATTTGCCAAGATAAAGGTCCTGCTCAATTTGAATATGTGTGGCAATTGGGATTTGCAGGATCTGAAGGC
  GAAAAGTGCCAAGGGGTTATTGATGCCTATTTCTTTCTGGCTGCAAACTGCACTGAAGATGCAACCTATG
  TGAACGATCCTGAAGATAATAATTCTTCATGTTGGTTCCCACATGAAGGCACAAAAGAGATTTGTGCAAA
  TGGATGCAGTTGTTTGAGTGAAGAAGACAGTCAGGAATATCGGTATCTATGTTTTCTCAGATGGGCTGGC
  AACATGTATCTGGAAAATACAACTGATGATCAAGAAAATGAGTGTCAACATGAAGCTGTTTGTAAAGATG
  AAATTAATAGACCCAGAAGAATCCTCAACACGGTGATACCACACCAAATTCAGCAACATATAGAAAGGTT
  TATACAGCATGACCAGGTGGGATTTATCGTAAGAATATAA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001142801
• ORF Size: 1860 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_001142801.1, NP_001136273.1
• RefSeq Size: 5462
• RefSeq ORF: 1860
• Locus ID: 346007
• Protein Families: Druggable Genome
• Gene Summary: The product of this gene contains multiple epidermal growth factor (EGF)-like and LamG domains. The protein is expressed in the photoreceptor layer of the retina, and the gene is mutated in autosomal recessive retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
  Transcript Variant: This variant (2) lacks several 3' exons but contains an alternate 3' terminal exon, and it thus differs in its 3' coding region and 3' UTR, compared to variant 1. The resulting isoform (2) has a substantially shorter and unique C-terminus, compared to isoform 1. 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.