n-Myc (MYCN) (NM_005378) Human Mutant ORF Clone

Specifications

Product Data
Product Name	n-Myc (MYCN) (NM_005378) Human Mutant ORF Clone
Mutation Description	S221X
Affected Codon#	221
Affected NT#	662
Nucleotide Mutation	MYCN Mutant (S221X), Myc-DDK-tagged ORF clone of Homo sapiens v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian) (MYCN) as transfection-ready DNA
Effect	Feingold syndrome
Synonyms	bHLHe37; MODED; N-myc; NMYC; ODED
Vector	pCMV6-Entry
Tag	Myc-DDK
ACCN	NM_005378
ORF Size	660 bp
Restriction Sites	SgfI-RsrII      Cloning Scheme for this gene
OTI Disclaimer	Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation	This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Reference Data
RefSeq	NP_005369
RefSeq Size	660 bp
RefSeq ORF	1395 bp
Locus ID	4613
Domains	HLH, Myc_N_term
Protein Families	Druggable Genome, Transcription Factors
MW	24.2 kDa
Gene Summary	This gene is a member of the MYC family and encodes a protein with a basic helix-loop-helix (bHLH) domain. This protein is located in the nucleus and must dimerize with another bHLH protein in order to bind DNA. Amplification of this gene is associated with a variety of tumors, most notably neuroblastomas. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]

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