SDHA (NM_004168) Human 3' UTR Clone

Specifications

Product Data
Product Name	SDHA (NM_004168) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CMD1GG; FP; MC2DN1; NDAXOA; PGL5; SDH1; SDH2; SDHF
ACCN	NM_004168
Insert Size	692 bp
Sequence Data	Insert Sequence (showhide) >SC203858 3’UTR clone of NM_004168 The sequence shown below is from the reference sequence of NM_004168. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACCGTCCCGCCAGCCATTCGCTCCTACTGATGAGACAAGATGTGGTGATGACAGAATCAGCTTTTGTAA TTATGTATAATAGCTCATGCATGTGTCCATGTCATAACTGTCTTCATACGCTTCTGCACTCTGGGGAAG AAGGAGTACATTGAAGGGAGATTGGCACCTAGTGGCTGGGAGCTTGCCAGGAACCCAGTGGCCAGGGAG CGTGGCACTTACCTTTGTCCCTTGCTTCATTCTTGTGAGATGATAAAACTGGGCACAGCTCTTAAATAA AATATAAATGAACAAACTTTCTTTTATTTCCAAATCCATTTGAAATATTTTACTGTTGTGACTTTAGTC ATATTTGTTGACCTAAAAATCAAATGTAATCTTTGTATTGTGTTACATCAAAATCCAGATATTTTGTAT AGTTTCTTTTTTCTTTTTCTTTTCTTTTTTTTTTTTGAGACAGGATCGGTGCAGTAGTACAATCACAGC TCACTGCAGCCTCAAACTCCTGGGCAGCTCAGGTGATCTTCCTGACTCAGCCTTCTGAGTAGTTGGGGC TACAGGTGTGCACCACCATGCCCAGCTCATTTATTTTGTAATTGTAGGGACAGGGTCTCACTGTGTTGC CTAGGCTGGTCTCAAGTGATCCTCCCTCCTTGGCCTCCCAAGGTGCTGGAATTATAGGTGTGAACAAAC CA 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_004168.4
Synonyms	CMD1GG; FP; MC2DN1; NDAXOA; PGL5; SDH1; SDH2; SDHF
Summary	This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]
Locus ID	6389
MW	26.6

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