MAGEL2 (NM_019066) Human Untagged Clone

SKU SC318105

MAGEL2 (untagged)-Human MAGE-like 2 (MAGEL2)

Product Data

• Type: Human Untagged Clone
• Target Symbol: MAGEL2
• Synonyms: NDNL1; nM15; PWLS; SHFYNG
• Vector: pCMV6 series
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_019066, the custom clone sequence may differ by one or more nucleotides; ATGGAATTCCAGGAGGTGCAGCAGACACAGGCGCTGGCCTGGCAGGCCCAGAAGGCCCCC; ACTCACATCTGGCAGCCCCTGCCTGCCCAGGAGGCCCAGAGGCAGGCTCCCCCCTTGGTC; CAGCTGGAGCAGCCCTTTCAGGGAGCCCCGCCCTCCCAAAAAGCCGTGCAAATCCAGCTA; CCCCCCCAGCAGGCCCAGGCATCGGGTCCGCAAGCGGAGGTGCCCACACTGCCGCTCCAG; CCTTCCTGGCAGGCACCGCCTGCAGTCTTGCAGGCCCAGCCCGGACCCCCGGTAGCAGCG; GCAAATTTTCCCCTGGGCTCCGCTAAATCATTGATGACTCCATCAGGAGAATGCAGGGCC; TCTTCTATAGACCGCAGGGGCTCCTCTAAAGAGCGCAGGACCTCCTCGAAGGAGCGCAGG; GCCCCTTCAAAAGACCGCATGATCTTTGCTGCCACCTTCTGTGCTCCCAAGGCAGTGTCA; GCTGCGCGAGCACACCTGCCAGCTGCCTGGAAAAACCTGCCTGCCACACCGGAGACCTTT; GCTCCCTCCTCAAGTGTCTTCCCAGCTACCTCCCAGTTTCAGCCTGCCTCTCTGAATGCC; TTTAAAGGCCCCTCTGCTGCCTCAGAGACCCCAAAGTCACTGCCATATGCTCTGCAGGAT; CCCTTTGCCTGTGTAGAGGCCCTGCCTGCAGTTCCATGGGTCCCACAGCCCAATATGAAT; GCCTCAAAGGCATCGCAGGCAGTGCCCACCTTCCTGATGGCTACAGCAGCTGCCCCCCAG; GCAACTGCCACCACTCAAGAGGCCTCCAAGACCTCCGTCGAGCCGCCACGCCGCTCCGGC; AAGGCCACCCGGAAGAAGAAGCATCTGGAAGCCCAAGAGGACAGCCGTGGCCACACGCTA; GCCTTTCATGACTGGCAGGGCCCAAGGCCCTGGGAGAATCTAAATCTGAGTGACTGGGAG; GTCCAAAGCCCTATCCAGGTCTCGGGTGACTGGGAGCACCCAAACACCCCCCGTGGCCTG; AGTGGTTGGGAGGGCCCTAGCACCTCCAGGATCCTGAGTGGCTGGGAAGGGCCCAGCGCA; TCCTGGGCCCTGAGTGCCTGGGAGGGCCCGAGCACCTCCAGGGCCCTGGGTCTCTCTGAA; AGCCCAGGGAGCTCTCTGCCCGTAGTTGTGTCTGAGGTCGCAAGTGTCTCTCCGGGATCC; AGTGCCACCCAGGATAATTCCAAGGTGGAGGCACAGCCCTTGTCTCCCTTGGATGAGAGG; GCAAATGCGTTGGTGCAGTTCCTCTTAGTCAAGGACCAAGCCAAGGTGCCTGTCCAGCGC; TCGGAGATGGTGAAAGTCATCCTCCGAGAGTATAAAGATGAGTGCTTAGATATCATCAAC; CGTGCCAACAATAAGCTGGAGTGTGCCTTTGGTTATCAATTGAAAGAAATTGATACCAAA; AACCACGCCTATATTATCATCAACAAGCTGGGCTACCATACAGGGAATTTGGTGGCATCC; TATTTAGACAGGCCCAAGTTTGGCCTTCTGATGGTGGTCTTGAGCCTCATCTTTATGAAA; GGCAACTGTGTCAGGGAGGATCTGATCTTTAATTTTCTGTTCAAGTTAGGGTTGGATGTC; CGGGAGACAAACGGTCTCTTTGGAAATACTAAGAAGCTCATCACCGAAGTGTTTGTCAGG; CAGAAGTACCTAGAGTACAGGCGAATCCCTTACACTGAGCCCGCAGAGTATGAGTTCCTC; TGGGGCCCTCGAGCATTCCTGGAAACCAGCAAGATGCTTGTCCTGAGGTTTTTGGCCAAG; CTCCATAAGAAAGATCCACAGAGCTGGCCATTCCATTACCTTGAAGCGCTCGCAGAGTGT; GAGTGGGAAGACACAGATGAGGATGAACCTGACACCGGTGACAGTGCCCACGGCCCCACC; AGCAGGCCCCCTCCCCGC;
• Restriction Sites: Please inquire
• ACCN: NM_019066
• Insert Size: 4298 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 TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.
• 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_019066.3, NP_061939.2
• RefSeq Size: 4298 bp
• RefSeq ORF: 1941 bp
• Locus ID: 54551
• UniProt ID: Q9UJ55
• Cytogenetics: 15q11.2
• Summary: Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010]