MAGEL2 (NM_019066) Human Untagged Clone

Specifications

Product Data
Type	Human Untagged Clone
Tag	Tag Free
Synonyms	NDNL1; nM15; PWLS; SHFYNG
Vector	pCMV6 series
Sequence Data	Fully Sequenced ORF (showhide) >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.
Product 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	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.
Reference Data
RefSeq	NM_019066.3, NP_061939.2
RefSeq Size	4298 bp
RefSeq ORF	1941 bp
Locus ID	54551
UniProt ID	Q9UJ55
Gene 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]

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.