NXNL2 (NM_145283) Human Untagged Clone

CAT#: SC123222

NXNL2 (untagged)-Human nucleoredoxin-like 2 (NXNL2), transcript variant 2

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: NXNL2
• Synonyms: C9orf121; RDCVF2; RdCVF2L
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for NM_145283 edited
  GTGTGGGCGGGGCGCAGTTGGGGGAGGGTGCAGAGACCTGAGGGCTTGAGGTTGCCTGGC
  TGGCCCCGCTCCCAGAGGCGGGTGCCGCGCTGTCGCCCAGGTATCTGGGGTCTCTGGTGT
  CTGAGTGTCTCATTGTCGGCGCGAACACAATTGCTCCAGCCACAGGCGAGGCCTGGCCAA
  GGTGTGGGCGCATCTAGGGCAGGTCTTGAGAGGTCCAGCGCCCGGTGGTGCGGACAGAGG
  CGGGGCACCGCGGCGCTCGCCGCCGCCTCCCCGCAGGTGATCATCCTCCTGCAGGTGTCC
  TCGGGTCTCAGGTGGCTGCGTGTCTGCGCCATGGTTGACATTCTGGGCGAGCGGCACCTG
  GTGACCTGTAAGGGCGCGACGGTGGAGGCCGAGGCGGCGCTGCAGAACAAGGTGGTGGCA
  CTGTACTTCGCGGCGGCCCGGTGCGCGCCGAGCCGCGACTTCACGCCGCTGCTCTGCGAC
  TTCTATACGGCGCTGGTGGCCGAGGCGCGGCGGCCCGCGCCCTTCGAAGTGGTCTTCGTG
  TCAGCCGACGGCAGCTGCCAGGAGATGCTGGACTTCATGCGCGAGCTGCATGGCGCCTGG
  CTGGCGCTGCCCTTCCACGACCCCTACCGGCAACGGAGTCTCGCTCTGTTGCCCAGGCTG
  GAGTGCAGTGGCGTGATCTTAGCTCACTGCAACCTTTGCCTCCTGGGTTCAAGTGATTCT
  CTAGCCTTAGCCTCCTGAGCATCTGGGACTACAGCCATTGCTGTGAATTACGTGAGGGAA
  AGATATTGAAGAGGAGTTGGACACTCCGAGAGTGCAGCTGTTCTCCCCCCGCACCATCCG
  TGTCCTGCATTCTGCGAGTCTGTGCTCATTAACAATGTGCTGTGACCATGTGACTCAGCA
  ATCCTGCTGCTGGGTATATACCCGAAAGAAAGGAAAAGGAAGCCAGTATATTGAAGAGGT
  ATCTGCACCCCCATGTTTATTGCAGCACTGTTCACAACAGCCAAGATTTGGAAGCAACCT
  AAGTGTCCATCAACAGATGAATGGATAAAGAAAACGTGGTACATATACACAATGGAGTAC
  TCTTCAGCCATTAAAAAAATGAGATTCTGTCATTTGCAATAATATAGATGGAAAAGGAGG
  CCCTTATGTGAAGTGAAATAAGCCAGGCACAGAAAGACAAACATCACATGTTCTCACTTA
  TTTGTGGGATCTAATGATCAAAACAATTGAACTCTTGGACATAGAGAGTAGAAGGTTGGT
  TACCAGAAGCTGGAAAGGAAAGTGGGGTTGGGAGGAAGGTGGGAATGGTTAATAGGTACA
  AAAAAATACAAAGAATAAATAAGACCTAATATTTGATAGCACAACAGTGTGACTACTGTC
  AATAATCATTTAATTGTACATTTAAAAATAACTATAATTGCATTGTTTGTAACACAAAAG
  ATAAATGCTTGAGGAGAAAAAAAAAAAAAAAA
  
  5' Read Nucleotide Sequence

  >OriGene 5' read for NM_145283 unedited
  AAATCTGCATTTGTAAACGACTTATATAGGCGGCCGCATCAACTTCTATAGCATACATTA
  TACTAAGTTATGGATCAGGCCAAATCGGCCGAGCTCGAATTCGTCGAGAGCGGGTGTGGG
  CGGGGCGCAGTTGGGGGAGGGTGCAGAGACCTGAGGGCTTGAGGTTGCCTGGCTGGCCCC
  GCTCCCAGAGGCGGGTGCCGCGCTGTCGCCCAGGTATCTGGGGTCTCTGGTGTCTGAGTG
  TCTCGTGTGTCGGCGCGAACACAATTGCTCCAGCCACAGGCGAGGCCTGGCCAAGGTGTG
  GGCGCATCTAGGGCAGGTCTTGAGAGGTCCAGCGCCCGGTGGTGCGGACAGAGGCGGGGC
  ACCGCGGCGCTCGCCGCCGCCTCCCCGCAGGTGATCATCCTCCTGCAGGTGTCCTCGGGT
  CTCAGGTGGCTGCGTGTCTGCGCCATGGTTGACATTCTGGGCGAGCGGCACCTGGTGACC
  TGTAAGGGCGCGACGGTGGAGGCCGAGGCGGCGCTGCAGAACAAGGTGGTGGCACTGTAC
  TTCGCGGCGGCCCGGTGCGCGCCGAGCCGCGACTTCACGCCGCTGCTCTGCGACTTCTAT
  ACGGCGCTGGTGGCCGAGGCGCGGCGGCCCGCGCCCTTCGAAGTGGTCTTCGTGTCAGCC
  GACGGCAGCTGCCAGGAGATGCTGGACTTCATGCGCGAGCTGCATGGCGCCTGGCTGGCG
  CTGCCCTTCCACGACCCCTACCGGCAACGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGC
  AGTGGCGTGATCTTAGCTCACTGCAACCTTTGCCTCCTGGGGTCAAGTGATTCTCTAGGC
  TTAGCCTCCTGAGCATCTGGGACTACAGCCATTGCTGTGGATTACTTGAGGGAAAGATAT
  TGAGAGGATTTGACACTCCGAG
  
• Restriction Sites: Please inquire
• ACCN: NM_145283
• ORF Size: 408 bp
• Insert Size: 1472
• 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_145283.1, NP_660326.1
• RefSeq Size: 1472
• RefSeq ORF: 408
• Locus ID: 158046
• Gene Summary: May be involved in the maintenance of both the function and the viability of sensory neurons, including photoreceptors and olfactory neurons. [UniProtKB/Swiss-Prot Function]
  Transcript Variant: This variant (2) differs in the 3' coding region and 3' UTR, compared to variant 1. The encoded isoform (2) has a distinct C-terminus and is shorter than 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.