SETDB2 (NM_031915) Human Untagged Clone

CAT#: SC127054

SETDB2 (untagged)-Human SET domain, bifurcated 2 (SETDB2), transcript variant 1


  "NM_031915" in other vectors (6)

Reconstitution Protocol

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    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol SETDB2
Synonyms C13orf4; CLLD8; CLLL8; KMT1F
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>NCBI ORF sequence for NM_031915, the custom clone sequence may differ by one or more nucleotides


ATGGGAGAAAAAAATGGCGATGCAAAAACTTTCTGGATGGAGCTAGAAGATGATGGAAAAGTGGACTTCA
TTTTTGAACAAGTACAAAATGTGCTGCAGTCACTGAAACAAAAGATCAAAGATGGGTCTGCCACCAATAA
AGAATACATCCAAGCAATGATTCTAGTGAATGAAGCAACTATAATTAACAGTTCAACATCAATAAAGGGA
GCATCACAGAAAGAAGTGAATGCCCAAAGCAGTGATCCTATGCCTGTGACTCAGAAGGAACAGGAAAACA
AATCCAATGCATTTCCCTCTACATCATGTGAAAACTCCTTTCCAGAAGACTGTACATTTCTAACAACAGA
AAATAAGGAAATTCTCTCTCTTGAAGATAAAGTTGTAGACTTTAGAGAAAAAGACTCATCTTCGAATTTA
TCTTACCAAAGTCATGACTGCTCTGGTGCTTGTCTGATGAAAATGCCACTGAACTTGAAGGGAGAAAACC
CTCTGCAGCTGCCAATCAAATGTCACTTCCAAAGACGACATGCAAAGACAAACTCTCATTCTTCAGCACT
CCACGTGAGTTATAAAACCCCTTGTGGAAGGAGTCTACGAAACGTGGAGGAAGTTTTTCGTTACCTGCTT
GAGACAGAGTGTAACTTTTTATTTACAGATAACTTTTCTTTCAATACCTATGTTCAGTTGGCTCGGAATT
ACCCAAAGCAAAAAGAAGTTGTTTCTGATGTGGATATTAGCAATGGAGTGGAATCAGTGCCCATTTCTTT
CTGTAATGAAATTGACAGTAGAAAGCTCCCACAGTTTAAGTACAGAAAGACTGTGTGGCCTCGAGCATAT
AATCTAACCAACTTTTCCAGCATGTTTACTGATTCCTGTGACTGCTCTGAGGGCTGCATAGACATAACAA
AATGTGCATGTCTTCAACTGACAGCAAGGAATGCCAAAACTTCCCCCTTGTCAAGTGACAAAATAACCAC
TGGATATAAATATAAAAGACTACAGAGACAGATTCCTACTGGCATTTATGAATGCAGCCTTTTGTGCAAA
TGTAATCGACAATTGTGTCAAAACCGAGTTGTCCAACATGGTCCTCAAGTGAGGTTACAGGTGTTCAAAA
CTGAGCAGAAGGGATGGGGTGTACGCTGTCTAGATGACATTGACAGAGGGACATTTGTTTGCATTTATTC
AGGAAGATTACTAAGCAGAGCTAACACTGAAAAATCTTATGGTATTGATGAAAACGGGAGAGATGAGAAT
ACTATGAAAAATATATTTTCAAAAAAGAGGAAATTAGAAGTTGCATGTTCAGATTGTGAAGTTGAAGTTC
TCCCATTAGGATTGGAAACACATCCTAGAACTGCTAAAACTGAGAAATGTCCACCAAAGTTCAGTAATAA
TCCCAAGGAGCTTACTGTGGAAACGAAATATGATAATATTTCAAGAATTCAATATCATTCAGTTATTAGA
GATCCTGAATCCAAGACAGCCATTTTTCAACACAATGGGAAAAAAATGGAATTTGTTTCCTCGGAGTCTG
TCACTCCAGAAGATAATGATGGATTTAAACCACCCCGAGAGCATCTGAACTCTAAAACCAAGGGAGCACA
AAAGGACTCAAGTTCAAACCATGTTGATGAGTTTGAAGATAATCTGCTGATTGAATCAGATGTGATAGAT
ATAACTAAATATAGAGAAGAAACTCCACCAAGGAGCAGATGTAACCAGGCGACCACATTGGATAATCAGA
ATATTAAAAAGGCAATTGAGGTTCAAATTCAGAAACCCCAAGAGGGACGATCTACAGCATGTCAAAGACA
GCAGGTATTTTGTGATGAAGAGTTGCTAAGTGAAACCAAGAATACTTCATCTGATTCTCTAACAAAGTTC
AATAAAGGGAATGTGTTTTTATTGGATGCCACAAAAGAAGGAAATGTCGGCCGCTTCCTTAATCATAGTT
GTTGCCCAAATCTCTTGGTACAGAATGTTTTTGTAGAAACACACAACAGGAATTTTCCATTGGTGGCATT
CTTCACCAACAGGTATGTGAAAGCAAGAACAGAGCTAACATGGGATTATGGCTATGAAGCTGGGACTGTG
CCTGAGAAGGAAATCTTCTGCCAATGTGGGGTTAATAAATGTAGAAAAAAAATATTATAA


>OriGene 5' read for NM_031915 unedited
GAATTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGCTGCGCTCGGG
AGGTTTGGGCGGCTTGGCGTCGGAGGAGAGCCCCACCCGCGGAGGAACCCAGCCTTGCCA
ACGGAGCTGGCGGAGCTCACTCCTCAGGTCAGGCGGGCGGCGTAGAAAACGCAGCGGAGC
CAGGTGAAACCAAGGCACCGCCGTGGCTGGCCCCCGACAGTTCCTCTAGCCGGGAGGTTG
GAGGAGCTGAAAACGCCGCGGAGCCCTCGGCCGCCCGAGCAGGGGCTGGACCCCAGCCCT
TGCAGCCTCCCTTCTCCTGGCACCCAAGTGCAGTCCTGGCTGCAGAAGGGGCCGCGGGCG
CACTGAGTTTCCAACCTCCATTTCAGCCTGTCTGTCTCAGGGTGCAGCCTTAATGAGAGG
TGATTCCTAAGCTGCTGGGAACCTGAGGTTGTCAAAGGGGCGGCAGGAAATGGACAGCAG
TATAAAACCCAGAAGCAGAACTTGAAGGTTAAACCACTAGCCCATTTCACAGGCGATGCA
AAAACTTTCTGGATGGAGCTAGAAGATGATGGAAAAGTGGACTTCATTTTTGAACAAGTA
CAAAATGTGCTGCAGTCACTGAAACAAAAGATCAAAGATGGGTCCTGCCACCAATAAAGA
ATACATCCAAGCAATGANTTCTAGTGAATGAAGCAAACTATATTAACAGTTCAACATCAT
AAAGGATCCTATGCCTGTGACTCAGAAGGACAGGAANACAATCCATGCATTTCCTCTACA
TATGTGAAACTNCTTTCAGAGACTGTCATTTCTACAACAGAATAGGAANTCTCTCTCTGA
AATAAGTGGTAACTTAAGAAAGACTATCTCGATTNACTACCAGGCTGAGCTCTGGGA
>OriGene 3' read for NM_031915 unedited
CGGCCGCAATCTAGAGTCGAGTTTTTTTTTTTTTTTTTTAATATTTTTTTTCTACATTTA
TTAACCCCACATTGGCAGAAGATTTCCTTCTCAGGCACAGTCCCAGCTTCATAGCCATAA
TCCCATGTTAGCTCTGTTCTTGCTTTCACATACCTGTTGGTGAAGAATGCCACCAATGGA
AAATTCCTGTTGTGTGTTTCTACAAAAACATTCTGTACCAAGAGATTTGGGCAACAACTA
TGATTAAGGAAGCGGCCGACATTTCCTTCTTTTGTGGCATCCAATAAAAACACATTCCCT
TTATTGAACTTTGTTAGAGAATCAGATGAAGTATTCTTGGTTTCACTTAGCAACTCTTCA
TCACAAAATACCTGCTGTCTTTGACATGCTGTAGATCGTCCCTCTTGGGGTTTCTGAATT
TGAACCTCAATTGCCTTTTTAATATTCTGATTATCCAATGTGGTCGCCTGGTTCTTCTGC
TCCTTGGTGGAGTTTCTTCTCTATATTTAGNTATATCTATCACATCTGATTCAATCACCA
GATTATCTTCAAACTCATCAACATGGTTTGAACTTGAGTCCTTTTGTGCTCCTTCGCTTT
TAGAGTTCAGATGCTCTCGGGGTGCTTTAAATCATCCTTTTTTTTTGAAGTGACCGACCT
CGAGAAACAAATTCATTTTTTTTCCATTGTGTTGAAAATGGCTGTCTTGATTCCGATCTT
TAAACCTGACGATTTGGATTCTTGACATATTTCCATATTCCGTTCCATAATAACCCCCTG
GGACCATTATGAACTTTGGGCGACTTTTCTTAATTTCCCACCCTCAGATTCGGGTTCCAT
CCCAAGGGAAAACTTCAATTTACAAACGGCCCCCCCCCTTCCACTTTTTTTTTTTAGAAA
CTACTTTTCAAGTATTTACATTTCCCGCGTGACAAACCCATTAAAAATTCGACGGAAACT
CTTTTTATACCTCCTTTCAAATCCCACAAGTTCTCTCCCCAGGTTTTAATCGTCCCCCCC
TTTCTTA
Restriction Sites NotI-NotI     
ACCN NM_031915
ORF Size 2160 bp
Insert Size 2600
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_031915.1, NP_114121.1
RefSeq Size 3307
RefSeq ORF 2160
Locus ID 83852
Domains SET, MBD, PreSET, Pre-SET
Protein Families Druggable Genome
Protein Pathways Lysine degradation
Gene Summary This gene encodes a member of a family of proteins that contain a methyl-CpG-binding domain (MBD) and a SET domain and function as histone methyltransferases. This protein is recruited to heterochromatin and plays a role in the regulation of chromosome segregation. This region is commonly deleted in chronic lymphocytic leukemia. Naturally-occuring readthrough transcription occurs from this gene to the downstream PHF11 (PHD finger protein 11) gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a). 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.

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