SPG7 (NM_003119) Human 3' UTR Clone

Specifications

Product Data
Product Name	SPG7 (NM_003119) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CAR; CMAR; PGN; SPG5C
ACCN	NM_003119
Insert Size	703 bp
Sequence Data	Insert Sequence (showhide) >SC208906 3’UTR clone of NM_003119 The sequence shown below is from the reference sequence of NM_003119. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGAGGCGAAGAGCCGACTTGGCCCAAGTAGTTGGGAGGTGTTGGCTGCACGTGCGGGTGGTCCGGGAAG TGAGGGCTCACTCAGCCACCCTGAGTTGCTTTTCAGCTGAGGTTTGCACTTCCTCTCGCGGCCCTCAGT AGTCCCTGCACAGTGACTTCTGAGATCTGTTGATTGATGACCCTTTTCATGATTTTAAGTTTCTCTGCA GAAACTACTGACGGAGTCCTGTGTTTGTGAGTCGTTTCCCCTATGGGGAAGGTTATCAGTGCTTCCCGA GTGAGCATGGAACACTTCGAGTTCCCAGGGTTATAGACAGTCGTTCCCAGTGTGGCTGAGGCCACCCAG AGGCAGCAGAGCATTCAGACTCCAAACAGACCCCTGTTCATGCCGACGCTTGCACGACCGCCCCAGTTC CTGTGGCTCCCTCGGAATGCTAAGGGGATCGGACATGAAAGGACCCTGTGAGCCGATTGTCCTATCTCC AGCGGCCCTGTCATCCAGCTCACTCATCAATGGGGCCAGTCAGGCCCAGGCACTGGGCTCCGGAGGACT CACCACTGCCCCCTGCTGCCATGTGGACTGGTGCAAGTTGAGGACTTCTTGCTGGTCTAGTCACGCATG CAGTGTTGGGGATGCCTTGGTTTTTACTGCTCTGAGAATTGTTGAGATACTTTACTAATAAACTGTGTA GTTGGAAAATCTA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_003119.4
Synonyms	CAR; CMAR; PGN; SPG5C
Summary	This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014]
Locus ID	6687
MW	25.3

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