DYRK1B (NM_004714) Human Untagged Clone

SKU SC323632

DYRK1B (untagged)-Kinase deficient mutant (K140M) of Human dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B (DYRK1B), transcript variant a

Product Data

• Type: Human Untagged Clone
• Target Symbol: DYRK1B
• Synonyms: AOMS3; MIRK
• Vector: pCMV6-XL4
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >OriGene ORF within SC323632 sequence for NM_004714 edited (data generated by NextGen Sequencing); ATGGCCGTCCCACCGGGCCATGGTCCCTTCTCTGGCTTCCCAGGGCCCCAGGAGCACACG; CAGGTATTGCCTGATGTGCGGCTACTGCCTCGGAGGCTGCCCCTGGCCTTCCGGGATGCA; ACCTCAGCCCCGCTGCGTAAGCTCTCTGTGGACCTCATCAAGACCTACAAGCACATCAAT; GAGGTATACTATGCGAAGAAGAAGCGGCGGGCCCAGCAGGCGCCACCCCAGGATTCGAGC; AACAAGAAGGAGAAGAAGGTCCTGAACCATGGTTATGATGACGACAACCATGACTACATC; GTGCGCAGTGGCGAGCGCTGGCTGGAGCGCTACGAAATTGACTCGCTCATTGGCAAAGGC; TCCTTTGGCCAGGTGGTGAAAGCCTATGATCATCAGACCCAGGAGCTTGTGGCCATCATG; ATCATCAAGAACAAAAAGGCTTTCCTGAACCAGGCCCAGATTGAGCTGCGGCTGCTGGAG; CTGATGAACCAGCATGACACGGAGATGAAGTACTATATAGTACACCTGAAGCGGCACTTC; ATGTTCCGGAACCACCTGTGCCTGGTATTTGAGCTGCTGTCCTACAACCTGTACGACCTC; CTGCGCAACACCCACTTCCGCGGCGTCTCGCTGAACCTGACCCGGAAGCTGGCGCAGCAG; CTCTGCACGGCACTGCTCTTTCTGGCCACGCCTGAGCTCAGCATCATTCACTGCGACCTC; AAGCCCGAAAACATCTTGCTGTGCAACCCCAAGCGCAGCGCCATCAAGATTGTGGACTTC; GGCAGCTCCTGCCAGCTTGGCCAGAGGATCTACCAGTATATCCAGAGCCGCTTCTACCGC; TCACCTGAGGTGCTCCTGGGCACACCCTACGACCTGGCCATTGACATGTGGTCCCTGGGC; TGCATCCTTGTGGAGATGCACACCGGAGAGCCCCTCTTCAGTGGCTCCAATGAGGTCGAC; CAGATGAACCGCATTGTGGAGGTGCTGGGCATCCCACCGGCCGCCATGCTGGACCAGGCG; CCCAAGGCTCGCAAGTACTTTGAACGGCTGCCTGGGGGTGGCTGGACCCTACGAAGGACG; AAAGAACTCAGGAAGGATTACCAGGGCCCCGGGACACGGCGGCTGCAGGAGGTGCTGGGC; GTGCAGACGGGCGGGCCCGGGGGCCGGCGGGCGGGGGAGCCGGGCCACAGCCCCGCCGAC; TACCTCCGCTTCCAGGACCTGGTGCTGCGCATGCTGGAGTATGAGCCCGCCGCCCGCATC; AGCCCCCTGGGGGCTCTGCAGCACGGCTTCTTCCGCCGCACGGCCGACGAGGCCACCAAC; ACGGGCCCGGCAGGCAGCAGTGCCTCCACCTCGCCCGCGCCCCTCGACACCTGCCCCTCT; TCCAGCACCGCCAGCTCCATCTCCAGTTCTGGAGGCTCCAGTGGCTCCTCCAGTGACAAC; CGGACCTACCGCTACAGCAACCGATATTGTGGGGGCCCTGGGCCCCCTATCACAGACTGT; GAGATGAACAGCCCCCAGGTCCCACCCTCCCAGCCGCTGCGGCCCTGGGCAGGGGGTGAT; GTGCCCCACAAGACACATCAAGCCCCTGCCTCTGCCTCGTCACTGCCTGGGACCGGGGCC; CAGTTACCCCCCCAGCCCCGATACCTTGGTCGTCCCCCATCACCAACCTCACCACCACCC; CCGGAGCTGATGGATGTGAGCCTGGTGGGCGGCCCTGCTGACTGCTCCCCACCTCACCCA; GCGCCTGCCCCCCAGCACCCGGCTGCCTCAGCCCTCCGGACTCGGATGACTGGAGGTCGT; CCACCCCTCCCGCCTCCTGATGACCCTGCCACTCTGGGGCCTCACCTGGGCCTCCGTGGT; GTACCCCAGAGCACAGCAGCCAGCTCGTGA; ; Clone variation with respect to NM_004714.1; 419 a=>t
  5' Read Nucleotide Sequence

  >OriGene 5' read for mutant NM_004714 unedited; GCGCCCGTTTGAGCAATTGGGCGGTAGGCGTGTACGGTGGGAGGTCTATATAAGCAGAGCTCGTTTAGTG; AACCGTCAGAATTTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGCCAGGGCGTGGG; GGGGCCGGTTTGTTGTGGTCGCCATTTTGCTGGTTGCATTACTGGGTAATCGGGGCCCTGGCTTGCCGCG; TCCGCCGGATACCCTCAGCCAGTGGGCAGGTCTGAGCTCGGGCTCCCCGAGCAGTTTGAGTCCCCTTGCC; CGCTCCTTCAGGTCTCAGCGGCGGTGGCAGCCGAGGTGCAGGGATGCAAGAAGCGCCCCCCCGGCCGGGC; TCCCGCTCCAGGCCTCGCTCCCCTGCGGCCCTCTGAGCCCAACCCATTGCCCGGTCCCCACCCGGGCAAT; TGTTCCCTTTCTCTGCCTCCCCAGGGCCCAGGAACCACCCCCCGGGATTTTGCCTGATGTGCGGCTACGG; CCTCGAAGGCTGCCCCTGCCCTTCGGGTTCCAACCTCGCCCCCGTTCCGTAGCCTTCTGGGGGACCTTAT; CGACCTTACGCCCACATCTGAGAGTGTACTCTGCGCAAAAAAAACCCGGGGCCCCGCGGGCCCCACCCCG; ATTTTCGCCCCACGGGAGGGAGAGAGGGCCGGAATGGGTTTTATGAGGACAACACGAGATATCTTGCGCA; CAGTGCGCACCGCTTCTGAACTCTAAAAATTGCTCTCTTGTGGAAAGGCTTTTTGCGCAGGTGGAAGACT; CTATATTCTACCACGAGCTGTGGCCTCTGATGTTATAACACAGCGTCTCATAACGCCCATAATCGCCGCT; GCTGGCGCCTGACACTGCACGCAGTGAAGACTTCTGTAGCTTAACAGCGCTATGCTGGACACCTGCCGCG; ATTGATAGCGTCGCACATGTGAGACTCGGCGAACCACTTC;
  Kinase Domain Sequence

  >SC323632 kinase domain raw sequence. By performing BLASTX analysis with this sequence against NCBI refernce protein database, you can confirm the presence of the kinase-deficient mutation; AGGCGRCGCTGGCTGGRCGCTACGAAATTGACTCGCTCATTGGCAAAGGCTCCTTTGGCCAGGTGGTGAA; AGCCTATGATCATCAGACCCAGGAGCTTGTGGCCATCATGATCATCAAGAACAAAAAGGCTTTCCTGAAC; CAGGCCCAGATTGAGCTGCGGCTGCTGGAGCTGATGAACCAGCATGACACGGAGATGAAGTACTATATAG; TACACCTGAAGCGGCACTTCATGTTCCGGAACCACCTGTGCCTGG;
• Restriction Sites: Please inquire
• ACCN: NM_004714
• Insert Size: 2487 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).
• OTI Annotation: This kinase-deficient mutant clone was generated by created by site-directed mutagenesis from the corresponding wild-type clone. See details in "Application of active and kinase-deficient kinome collection for identification of kinases regulating hedgehog signaling." Cell. 2008 May p536-548.
• 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 Method: 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.
• Note: Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required.
• Shipping: Ambient

Reference Data

• RefSeq: NM_004714.1, NP_004705.1
• RefSeq Size: 2540 bp
• RefSeq ORF: 1890 bp
• Locus ID: 9149
• UniProt ID: Q9Y463
• Cytogenetics: 19q13.2
• Protein Families: Druggable Genome, Protein Kinase, Transcription Factors
• Summary: This gene encodes a member of a family of nuclear-localized protein kinases. The encoded protein participates in the regulation of the cell cycle. Expression of this gene may be altered in tumor cells, and mutations in this gene were found to cause abdominal obesity-metabolic syndrome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]; Transcript Variant: This variant (1, also known as 'a') represents the longest transcript and encodes the longest isoform (p69, also known as isoform a).