Slc39a14 (NM_144808) Mouse Untagged Clone

CAT#: MC216883

Slc39a14 (untagged) - Mouse solute carrier family 39 (zinc transporter), member 14 (Slc39a14), transcript variant 3, (10ug)

Specifications

Product Data

• Type: Mouse Untagged Clone
• Tag: Tag Free
• Symbol: Slc39a14
• Synonyms: FAD-123; fad123; ZIP-14; Zip14
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >MC216883 representing NM_144808
  Red=Cloning site Blue=ORF Orange=Stop codon
  
  TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC
  GCCGCGATCGCC
  
  ATGAAGCGGCTGCACCCAGCCCTTCCAAGCTGCCTCCTGTTGGTGCTGTTTGGTATATGGAGAACTGCCC
  CCCAGACTCATGCCTCGTCTGCTGGCCTGCCGCCCCTCAGTGCCACCTCCTTCCTGGAAGATCTCATGGA
  CCGCTATGGAAAGAATGACAGCCTTACCCTGACACAGCTGAAGTCCCTGCTCGACCACCTGCATGTGGGA
  GTGGGCCGGGATAATGTTTCCCAGCCCAAGGAAGGACCCAGGAACCTCTCCACGTGCTTTAGCTCTGGAG
  ACCTCTTTGCGGCGCACAACTTGAGCGAGCGATCTCAGATCGGGGCGAGTGAGTTCCAGGAGTTCTGCCC
  CACCATTCTCCAGCAGCTGGATTCCCAGGCCTGCACCTCAGAAAACCAGAAGTCTGAGGAGAATGAACAG
  ACAGAGGAGGGGAAGCCAAGCGCCATTGAAGTATGGGGGTACGGTTTCCTCTGCGTTACCGTCATCTCCC
  TCTGCTCCCTCATGGGGGCCAGCGTGGTGCCCTTCATGAAGAAGACTTTTTACAAGAGGCTCCTGCTCTA
  CTTCATAGCCTTGGCGATTGGAACCCTCTACTCCAACGCCCTCTTCCAGCTCATCCCAGAGGCTTTTGGC
  TTCAACCCTCAGGACAATTACGTCTCCAAGTCTGCAGTGGTGTTTGGGGGTTTCTACCTTTTCTTTTTCA
  CAGAAAAGATCCTGAAGATGCTCTTGAAGCAGAAAAACGAGCACCATCACGGGCATAACCATTTTACCTC
  CGAGACACTTCCTTCCAAGAAGGACCAGGAGGAGGGTGTGACCGAGAAGCTACAGAACGGGGACCTGGAT
  CACATGATCCCTCAGCACTGCAACAGCGAGCTGGATGGCAAGGCGCCTGGCACGGACGAGAAGGTCATTG
  TCAACTCCATGTCTGTGCAGGACCTGCAGGCATCCCAGAGTGCTTGCTACTGGCTCAAGGGGGTCCGCTA
  CTCTGATATCGGGACCTTGGCCTGGATGATCACCCTGAGCGATGGGCTCCACAATTTCATCGATGGCCTG
  GCTATTGGTGCCTCCTTCACTGTGTCTGTCTTCCAAGGCATCAGCACGTCAGTGGCCATTCTCTGTGAGG
  AATTCCCTCATGAGCTGGGAGACTTCGTCATCCTGCTCAATGCTGGCATGAGCATCCAGCAGGCTCTCTT
  CTTCAACTTCCTCTCTGCCTGCTGCTGCTATTTGGGTCTGGCCTTTGGCATCCTGGCTGGCAGCCACTTC
  TCTGCAAACTGGATTTTTGCACTGGCTGGAGGAATGTTCTTGTATATTGCCCTAGCCGATATGTTCCCTG
  AGATGAATGAAGTCTGCCAGGAGGATGAGAAGAACGACAGCTTTCTGGTCCCCTTTGTCATCCAGAATCT
  TGGCCTCCTAACCGGCTTCTCCATTATGCTGGTCCTCACAATGTATTCAGGGCAGATTCAGATCGGGTAG
  
  ACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCCTGGATT
  ACAAGGATGACGACGATAAGGTTTAA
• Restriction Sites: SgfI-MluI
• ACCN: NM_144808
• Insert Size: 1470 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).
• Product Components: The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
• Reconstitution: 1. Centrifuge at 5,000xg for 5min.
  2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
  3. Close the tube and incubate for 10 minutes at room temperature.
  4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
  5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.

Reference Data

• RefSeq: NM_144808.4, NP_659057.2
• RefSeq Size: 4927 bp
• RefSeq ORF: 1470 bp
• Locus ID: 213053
• UniProt ID: Q75N73
• Cytogenetics: 14 D2
• Gene Summary: Broad-scope metal ion transporter with a preference for zinc uptake. Also mediates cellular uptake of nontransferrin-bound iron.[UniProtKB/Swiss-Prot Function]
  Transcript Variant: This variant (3) lacks an in-frame exon and contains an alternate in-frame exon in the central coding region, compared to variant 1. The encoded isoform (b) is the same length as isoform a, but contains a distinct internal segment. 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.