IRAK4 (NM_016123) Human Untagged Clone

SKU SC323644

IRAK4 (untagged)-Kinase deficient mutant (K213M) of Human interleukin-1 receptor-associated kinase 4 (IRAK4), transcript variant 2

Product Data

• Type: Human Untagged Clone
• Target Symbol: IRAK4
• Synonyms: IMD67; IPD1; IRAK-4; NY-REN-64; REN64
• Vector: pCMV6-XL5
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: None
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_016123, the custom clone sequence may differ by one or more nucleotides; ; ; ATGAACAAACCCATAACACCATCAACATATGTGCGCTGCCTCAATGTTGGACTAATTAGGAAGCTGTCAG; ATTTTATTGATCCTCAAGAAGGATGGAAGAAGTTAGCTGTAGCTATTAAAAAACCATCTGGTGATGATAG; ATACAATCAGTTTCACATAAGGAGATTTGAAGCATTACTTCAAACTGGAAAAAGTCCCACTTCTGAATTA; CTGTTTGACTGGGGCACCACAAATTGCACAGTTGGTGATCTTGTGGATCTTTTGATCCAAAATGAATTTT; TTGCTCCTGCGAGTCTTTTGCTCCCAGATGCTGTTCCCAAAACTGCTAATACACTACCTTCTAAAGAAGC; TATAACAGTTCAGCAAAAACAGATGCCTTTCTGTGACAAAGACAGGACATTGATGACACCTGTGCAGAAT; CTTGAACAAAGCTATATGCCACCTGACTCCTCAAGTCCAGAAAATAAAAGTTTAGAAGTTAGTGATACAC; GTTTTCACAGTTTTTCATTTTATGAATTGAAGAATGTCACAAATAACTTTGATGAACGACCCATTTCTGT; TGGTGGTAATAAAATGGGAGAGGGAGGATTTGGAGTTGTATATAAAGGCTACGTAAATAACACAACTGTG; GCAGTGAAGAAGCTTGCAGCAATGGTTGACATTACTACTGAAGAACTGAAACAGCAGTTTGATCAAGAAA; TAAAAGTAATGGCAAAGTGTCAACATGAAAACTTAGTAGAACTACTTGGTTTCTCAAGTGATGGAGATGA; CCTCTGCTTAGTATATGTTTACATGCCTAATGGTTCATTGCTAGACAGACTCTCTTGCTTGGATGGTACT; CCACCACTTTCTTGGCACATGAGATGCAAGATTGCTCAGGGTGCAGCTAATGGCATCAATTTTCTACATG; AAAATCATCATATTCATAGAGATATTAAAAGTGCAAATATCTTACTGGATGAAGCTTTTACTGCTAAAAT; ATCTGACTTTGGCCTTGCACGGGCTTCTGAGAAGTTTGCCCAGACAGTCATGACTAGCAGAATTGTGGGA; ACAACAGCTTATATGGCACCAGAAGCTTTGCGTGGAGAAATAACACCCAAATCTGATATTTACAGCTTTG; GTGTGGTTTTACTAGAAATAATAACTGGACTTCCAGCTGTGGATGAACACCGTGAACCTCAGTTATTGCT; AGATATTAAAGAAGAAATTGAAGATGAAGAAAAGACAATTGAAGATTATATTGATAAAAAGATGAATGAT; GCTGATTCCACTTCAGTTGAAGCTATGTACTCTGTTGCTAGTCAATGTCTGCATGAAAAGAAAAATAAGA; GACCAGACATTAAGAAGGTTCAACAGCTGCTGCAAGAGATGACAGCTTCTTAA; ;
  5' Read Nucleotide Sequence

  >OriGene 5' read for mutant NM_016123 unedited; ACCGCCCGTTGAGCAATGGGCGGTAGGCGTGTACGGTGGGAGGTCTATATAAGCAGAGCTCGTTTAGTGA; ACCGTCAGAATTTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGGTTCTTCTGTCGC; CGGCTTCAGCAGCCCGCGCCCGGGCAGGAATAGAAGATGAACAAACCCATAACACCATCAACATATGTGC; GCTGCCTCAATGTTGGACTAATTAGGAAGCTGTCAGATTTTATTGATCCTCAAGAAGGATGGAAGAAGTT; AGCTGTAGCTATTAAAAAACCATCTGGTGATGATAGATACAATCAGTTTCACATAAGGGAGATTTGAAGC; ATTACTTCAAACTGGAAAAAGTCCCCACTTCTGATTTACTGTTTGACTGGGGGCACCACCAATTGTGCAC; AGTTGGTGTAATCTTTGTGGGGATCTTTTGAGATCCCAAAATGAAATTTTTTGCTTCCGCGCGATCTCTT; TGGCTCCAGAAATGCCTGGTTCCCAAAACTGCTAAACCACTACTTCTCTAAGAAAAGCTAAAACAGTCCG; ACCAAAAACAATGGCCTTTTCTGTGACAGACACGAGAATTGGGGCACCCTCGGTCGAAAACTTTTACAAA; AGCTATTATACCCCACCCGCACCCCCAATGCCCGAAAAAAAAAGTTTTAAAATTTTAGGGATACCGTTTT; ACACGATTTTTCATTTTTAAAATGTGAAAAAAGTGCCAAAAAACATTTTTGGAAAAACCACCCTTTGTGG; GTGGTGGATATAAAATGAAAAGAGAATATTTTGTTGTTTTAAAGGGGCCTCATACACACTGTGGTGGGGG; AGACATGCTGCACGGTTGTATACTACTGCGAATGAGCACCGTTGTTTCTAAAAAAAAATGGCGAGAGTGT; GCCGAGAACACTTGACACTCCGTTGTCACTGATGAGAGACACACCGCTACTATAGTTATATCCCCGCGTG; TTGTCCG;
  Kinase Domain Sequence

  >SC323644 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; CMCTTCTGTTGGTGGTATAAATGGGAGAGGGAGGATTTGGAGTTGTATATAAAGGCTACGTAAATAACAC; AACTGTGGCAGTGATGAAGCTTGCAGCAATGGTTGACATTACTACTGAAGAACTGAAACAGCAGTTTGAT; CAAGAAATAAAAGTAATGGCAAAGTGTCAACATGAAAACTTAGTAGAACTACTTGGTTTCTCAAGTGATG; GAGATGACCTCTGCTTAGTATATGTTTACATGCCTAATGGTTCAT;
• Restriction Sites: Please inquire
• ACCN: NM_016123
• Insert Size: 3000 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_016123.1, NP_057207.1
• RefSeq Size: 2817 bp
• RefSeq ORF: 1383 bp
• Locus ID: 51135
• UniProt ID: Q9NWZ3
• Cytogenetics: 12q12
• Domains: DEATH, pkinase, S_TKc, TyrKc
• Protein Families: Druggable Genome, Protein Kinase
• Protein Pathways: Apoptosis, Neurotrophin signaling pathway, Toll-like receptor signaling pathway
• Summary: This gene encodes a kinase that activates NF-kappaB in both the Toll-like receptor (TLR) and T-cell receptor (TCR) signaling pathways. The protein is essential for most innate immune responses. Mutations in this gene result in IRAK4 deficiency and recurrent invasive pneumococcal disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]; Transcript Variant: This variant (2) differs in the 5' UTR compared to variant 1. Variants 1, 2, and 13 all encode the same 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.