Dph3 (NM_172254) Mouse Untagged Clone

CAT#: MC202244

Dph3 (untagged) - Mouse DPH3 homolog (KTI11, S. cerevisiae) (Dph3), transcript variant 1, (10ug)

Specifications

Product Data

• Type: Mouse Untagged Clone
• Tag: Tag Free
• Symbol: Dph3
• Synonyms: DELGIP1; DelgipP1; Desr1; KTI11; Zcsl2
• Vector: PCMV6-Kan/Neo
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >BC029910 sequence for NM_172254
  GGAAGACCGGGCCTTACCCTGCCTGGGCGCAGGTAGGCAAGCTGATGCGGTGCCGACCGGGTGACCATGG CGGTGTTTCACGACGAGGTGGAGATCGAGGACTTTCAATATGACGAGGACTCGGAGACATATTTCTACCC TTGCCCCTGTGGGGATAACTTTGCCATCACCAAGGAAGATTTGGAAAATGGAGAAGATGTGGCCACGTGT CCTAGCTGCTCACTCATTATAAAAGTGATTTATGACAAAGATCAGTTCATGTGTGGAGAAACAGTCCCAG CACCTTCAACCAACAAGGAGTTAGTTAAATGCTGAAGAGGCTCTCAGGTACCCACATCCTGAACCGTGGG GGCTGAGCCCAGGTGGATGGATCCAGTGCAGAGTTACCAACCTCCTCGATGGGCAGCCTCAGGGGTGTGA TCTTCATCAGCCACTGAACTCAGCATGAAAAAGGGAGCCTATGACATGCCAGCCCTGGATTCCATACTGG GACTGGAAGGATTCCTAATTGTCCGTCTGAATTTAAGGAAGAGCCTTATTATAAACTGTGGTTTTTCCTT CAGTCGGCTGCATCATTTGAACATCTGGAAATTCATTTTCTGAAAATAACATCATCCGCCTCAAAAAAAA AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
• Restriction Sites: RsrII-NotI
• ACCN: NM_172254
• ORF Size: 249 bp
• Insert Size: 249
• 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: BC029910, AAH29910
• RefSeq Size: 677
• RefSeq ORF: 249
• Locus ID: 105638
• Gene Summary: Essential for the first step in the synthesis of diphthamide, a post-translational modification of histidine which occurs in elongation factor 2. [UniProtKB/Swiss-Prot Function]
  Transcript Variant: This variant (1) encodes the longer isoform (1). Both variants 1 and 3 encode the same isoform. 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.