Tuberin (TSC2) (NM_000548) Human Mutant ORF Clone

Specifications

Product Data
Product Name	Tuberin (TSC2) (NM_000548) Human Mutant ORF Clone
Mutation Description	K7X
Affected Codon#	7
Affected NT#	19
Nucleotide Mutation	TSC2 Mutant (K7X), Myc-DDK-tagged ORF clone of Homo sapiens tuberous sclerosis 2 (TSC2), transcript variant 1 as transfection-ready DNA
Effect	Tuberous slerosis
Synonyms	LAM; PPP1R160; TSC4
Vector	pCMV6-Entry
Tag	Myc-DDK
ACCN	NM_000548
ORF Size	18 bp
Sequence Data	ORF Nucleotide Sequence (showhide) >RC402303 representing NM_000548 Red=Cloning site Blue=ORF Green=Tags(s) TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC GCCGCGATCGCC ATGGCCAAACCAACAAGC AGCGGACCGACGCGTACGCGGCCGCTCGAGCAGAAACTCATCTCAGAAGAGGATCTGGCAGCAAATGATATCC TGGATTACAAGGATGACGACGA TAAGGTTTAA Protein Sequence (showhide) >RC402303 representing NM_000548 Red=Cloning site Green=Tags(s) MAKPTS SGPTRTRRLEQKLISEEDLAANDILDYKDDDDKV
Restriction Sites	SgfI-XhoI      Cloning Scheme for this gene
OTI Disclaimer	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_000539
RefSeq Size	18 bp
RefSeq ORF	5424 bp
Locus ID	7249
Domains	Rap_GAP, Tuberin
Protein Families	Druggable Genome
Protein Pathways	Insulin signaling pathway, mTOR signaling pathway, p53 signaling pathway
MW	0.7 kDa
Gene Summary	Mutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

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