SUV420h1 (KMT5B) (NM_001300908) Human Untagged Clone

CAT#: SC337085

SUV420H1 (untagged) - Human suppressor of variegation 4-20 homolog 1 (Drosophila) (SUV420H1), transcript variant 4


  "NM_001300908" in other vectors (1)

Reconstitution Protocol

USD 660.00

3 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol KMT5B
Synonyms CGI-85; CGI85; MRD51; SUV420H1
Vector pCMV6-Entry
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>NCBI ORF sequence for NM_001300908, the custom clone sequence may differ by one or more nucleotides


ATGCTACTTAGACATGGAGAAAACGACTTCAGTGTCATGTACTCCACAAGGAAAAACTGTGCTCAACTCT
GGCTGGGTCCTGCTGCGTTTATAAACCATGATTGCAGACCTAATTGTAAGTTTGTGTCAACTGGTCGAGA
TACAGCATGTGTGAAGGCTCTAAGAGACATTGAACCTGGAGAAGAAATTTCTTGTTATTATGGAGATGGG
TTCTTTGGAGAAAATAATGAGTTCTGCGAGTGTTACACTTGCGAAAGACGGGGCACTGGTGCTTTTAAAT
CCAGAGTGGGACTGCCTGCGCCTGCTCCTGTTATCAATAGCAAATATGGACTCAGAGAAACAGATAAACG
TTTAAATAGGCTTAAAAAGTTAGGTGACAGCAGCAAAAATTCAGACAGTCAATCTGTCAGCTCTAACACT
GATGCAGATACCACTCAGGAAAAAAACAATGCAACTTCTAACCGAAAATCTTCAGTTGGCGTAAAAAAGA
ATAGCAAGAGCAGAACGTTAACGAGGCAATCTATGTCAAGAATTCCAGCTTCTTCCAACTCTACCTCATC
TAAGCTAACTCATATAAATAATTCCAGGGTACCAAAGAAACTGAAGAAGCCTGCAAAGCCTTTACTTTCA
AAGATAAAATTGAGAAATCATTGCAAGCGGCTGGAGCAAAAGAATGCTTCAAGAAAACTCGAAATGGGAA
ACTTAGTACTGAAAGAGCCTAAAGTAGTTCTGTATAAAAATTTGCCCATTAAAAAAGATAAGGAGCCAGA
GGGACCAGCCCAAGCCGCAGTTGCCAGCGGGTGCTTGACTAGACACGCGGCGAGAGAACACAGACAGAAT
CCTGTGAGAGGTGCTCATTCGCAGGGGGAGAGCTCGCCCTGCACCTACATAACTCGGCGGTCAGTGAGGA
CAAGAACAAATCTGAAGGAGGCCTCTGACATCAAGCTTGAACCAAATACGTTGAATGGCTATAAAAGCAG
TGTGACGGAACCTTGCCCCGACAGTGGTGAACAGCTGCAGCCAGCTCCTGTGCTGCAGGAGGAAGAACTG
GCTCATGAGACTGCACAAAAAGGGGAGGCAAAGTGTCATAAGAGTGACACAGGCATGTCCAAAAAGAAGT
CACGACAAGGAAAACTTGTGAAACAGTTTGCAAAAATAGAGGAATCTACTCCAGTGCACGATTCTCCTGG
AAAAGACGACGCGGTACCAGATTTGATGGGTCCCCATTCTGACCAGGGTGAGCACAGTGGCACTGTGGGC
GTGCCTGTGAGCTACACAGACTGTGCTCCTTCACCCGTCGGTTGTTCAGTTGTGACATCAGATAGCTTCA
AAACAAAAGACAGCTTTAGAACTGCAAAAAGTAAAAAGAAGAGGCGAATCACAAGGTATGATGCACAGTT
AATCCTAGAAAATAACTCTGGGATTCCCAAATTGACTCTTCGTAGGCGTCATGATAGCAGCAGCAAAACA
AATGACCAAGAGAATGATGGAATGAACTCTTCCAAAATAAGCATCAAGTTAAGCAAAGACCATGACAACG
ATAACAATCTCTATGTAGCAAAGCTTAATAATGGATTTAACTCAGGATCAGGCAGTAGTTCTACAAAATT
AAAAATCCAGCTAAAACGAGATGAGGAAAATAGGGGGTCTTATACAGAGGGGCTTCATGAAAATGGGGTG
TGCTGCAGTGATCCTCTTTCTCTCTTGGAGTCTCGAATGGAGGTGGATGACTATAGTCAGTATGAGGAAG
AAAGTACAGATGATTCCTCCTCTTCTGAGGGCGATGAAGAGGAGGATGACTATGATGATGACTTTGAAGA
CGATTTTATTCCTCTTCCTCCAGCTAAGCGCTTGAGGTTAATAGTTGGAAAAGACTCTATAGATATTGAC
ATTTCTTCAAGGAGAAGAGAAGATCAGTCTTTAAGGCTTAATGCCTAA


Restriction Sites SgfI-MluI     
ACCN NM_001300908
ORF Size 1938 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_001300908.1, NP_001287837.1
RefSeq Size 5802
RefSeq ORF 1938
Locus ID 51111
Protein Families Druggable Genome
Protein Pathways Lysine degradation
Gene Summary This gene encodes a protein that contains a SET domain. SET domains appear to be protein-protein interaction domains that mediate interactions with a family of proteins that display similarity with dual-specificity phosphatases (dsPTPases). The function of this gene has not been determined. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Transcript Variant: This variant (4) uses an alternate first exon and an alternate splice junction at the 5' end of an exon, and uses a downstream start codon compared to variant 1. The resulting isoform (4) is shorter at the N-terminus 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.

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