SEMA4F (NM_001271662) Human Untagged Clone

CAT#: SC330951

SEMA4F (untagged) - Homo sapiens sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F (SEMA4F), transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SEMA4F
• Synonyms: M-SEMA; m-Sema-M; PRO2353; S4F; SEMAM; SEMAW
• Vector: pCMV6 series
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001271662, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGCCGGCCTCTGCTGCGCGGCCCCGCCCGGGTCCCGGGCAGCCTACAGCCTCGCCCTTCCCGCTACTGC
  TGCTGGCGGTGCTGAGCGGCCCGGTATCCGGCCGCGTCCCCCGCTCGGTGCCCAGAACCTCGCTTCCAAT
  CTCTGAGGCTGACTCCTGTCTCACCCGGTTCGCAGTCCCTCACACATACAATTACTCTGTTCTCCTTGTG
  GATCCTGCCTCCCACACACTTTATGTTGGCGCCCGGGACACCATCTTCGCTTTATCCCTGCCCTTCTCAG
  GGGAGAGACCCCGCAGGATTGACTGGATGGTTCCTGAGGCTCACAGACAGAACTGTAGGAAGAAAGGCAA
  GAAAGAGGATGTGTCCAGGTTCCAGCAGGTTGAAAGACTTGAGAGTGGCCGGGGGAAATGTCCTTTTGAG
  CCAGCTCAGCGGTCAGCAGCTGTAATGGCTGGGGGGGTCCTCTATGCTGCCACTGTGAAAAACTACCTGG
  GGACGGAGCCAATTATCACCAGAGCAGTGGGTCGTGCCGAGGACTGGATTCGGACAGATACCTTGCCTTC
  CTGGCTGAACGCCCCAGCCTTTGTCGCAGCCGTGGCCTTGAGCCCAGCCGAATGGGGGGATGAAGATGGA
  GACGACGAAATCTACTTCTTCTTTACGGAGACTTCCCGAGCATTTGACTCATACGAGCGCATTAAAGTCC
  CACGGGTGGCCCGTGTGTGTGCGGGGGACCTCGGGGGCCGGAAGACCCTCCAGCAGAGATGGACGACGTT
  TTTGAAAGCTGACCTGCTCTGTCCAGGGCCTGAGCATGGCCGGGCCTCCAGTGTCCTGCAGGATGTTGCT
  GTGCTTCGACCTGAGCTTGGGGCAGGGACTCCCATCTTTTATGGCATCTTTTCTTCCCAGTGGGAGGGGG
  CTACTATCTCTGCTGTCTGTGCCTTCCGACCACAAGACATTCGGACAGTGCTGAATGGTCCCTTCAGAGA
  ACTAAAACATGACTGCAACAGAGGACTGCCTGTCGTGGACAATGATGTGCCCCAGCCCAGACCTGGAGAG
  TGCATCACCAACAACATGAAGCTCCGGCACTTTGGCTCATCTCTCTCCCTGCCTGACCGCGTACTCACCT
  TCATCCGGGACCACCCACTCATGGACAGGCCAGTGTTTCCAGCTGATGGCCACCCCCTGCTGGTCACTAC
  AGATACAGCCTATCTCAGAGTCGTGGCCCACAGGGTGACCAGCCTCTCAGGGAAAGAGTATGATGTGCTC
  TACCTGGGGACAGAGGATGGACACCTCCACCGAGCAGTGCGGATCGGAGCTCAGCTCAGCGTTCTTGAAG
  ATCTGGCCTTATTCCCAGAGCCACAGCCAGTTGAGAACATGAAATTGTACCACAGCTGGCTCCTGGTTGG
  CTCCCGTACTGAGGTGACACAAGTGAATACAACCAACTGTGGCCGTCTCCAGAGCTGCTCAGAGTGCATC
  CTGGCCCAGGACCCAGTCTGTGCCTGGAGCTTCCGGCTGGATGAGTGTGTGGCCCATGCCGGGGAGCACC
  GAGGGTTGGTCCAAGACATAGAGTCAGCAGATGTCTCCTCTTTGTGTCCTAAAGAGCCTGGAGAACGTCC
  AGTAGTGTTTGAAGTTCCCGTGGCTACAGCTGCGCATGTGGTCTTGCCATGTTCTCCAAGCTCAGCATGG
  GCATCCTGTGTGTGGCACCAGCCCAGTGGAGTGACTGCACTCACCCCCCGGCGGGATGGACTGGAGGTGG
  TGGTGACCCCAGGGGCCATGGGCGCTTATGCCTGTGAATGTCAGGAGGGTGGGGCAGCCCATGTGGTAGC
  AGCTTACAGCTTGGTATGGGGCAGCCAGCGAGATGCTCCGAGCCGGGCCCACACAGTGGGGGCGGGACTG
  GCTGGCTTCTTCTTGGGGATTCTCGCAGCATCCCTGACTCTCATTCTGATTGGTCGGCGTCAGCAGCGAC
  GGCGACAGAGGGAACTTCTGGCTAGAGACAAGGTGGGCCTGGACCTGGGGGCTCCACCTTCTGGGACCAC
  AAGCTACAGCCAAGACCCTCCCTCCCCCTCTCCTGAAGATGAGCGGTTGCCGCTGGCCCTGGCCAAGAGG
  GGCAGTGGCTTTGGTGGATTCTCACCACCCTTCCTGCTTGATCCTTGCCCAAGCCCAGCCCACATTCGGC
  TAACTGGGGCTCCTCTAGCCACATGTGATGAAACATCCATCTAG
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001271662
• ORF Size: 2214 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).

Reference Data

• RefSeq: NM_001271662.1, NP_001258591.1
• RefSeq Size: 6023
• RefSeq ORF: 2214
• Locus ID: 10505
• Protein Families: Transmembrane
• Protein Pathways: Axon guidance
• Gene Summary: This gene encodes a transmembrane class IV semaphorin family protein, which plays a role in neural development. This gene may be involved in neurogenesis in prostate cancer, the development of neurofibromas, and breast cancer tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]
  Transcript Variant: This variant (3) lacks an internal in-frame exon in the coding region, compared to variant 1. The encoded isoform (3) is shorter, 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.