AFG3L2 (NM_006796) Human 3' UTR Clone
CAT#: SC206154
3' UTR clone of AFG3 ATPase family gene 3-like 2 (yeast) (AFG3L2) nuclear gene encoding mitochondrial protein for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
Cited in 1 publication. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | AFG3L2 (NM_006796) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | OPA12; SCA28; SPAX5 |
ACCN | NM_006796 |
Insert Size | 651 bp |
Sequence Data |
>SC206154 3’UTR clone of NM_006796
The sequence shown below is from the reference sequence of NM_006796. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAGCCCCCGGGTGAGAAAGTTGCCAACTAGAGGCCCAGAGGGAGGCCATCTCAGTCTGTCCACTGTGGT TTCAGCTGGTGCATTATTTCAGCTGTGGCTTTCAGAAGAATGGGAATGCTGCGCTGATTTTAGCCAGCC ACTGGCCCAGCTGAAATGATGGGGAAAGGAGTCCTTAGTCCTTTCAGCCTCAGAGGTCACAGTGGGTGG CAGGTGACTTTCCGGAGGCCTTGAGGGAAATGCACACTGTCCCATAGCCTCATTGGGCTCCCAGACGTG CTGGAAAGGTTGAGCCCAGAGTGGCCGAGGCTGGACCCTGTGGCACCAAGTGGGGTCGGCTGACCGTGT GGCAGGGATCGTTGCACTGGACTCTTGGCGTGTGGGAAGGGATGCTTTCTCTTTGTCGCCCACTCTTCA TTCCTGTTTCTCCTCAGTTCCCCTGTGCAGATGGGCTGTGAAATTAAATTGGAGTCTTGATAAGAACAT TTTAATTTGACTTAATATTTTAAAGATTGAATCCAGATCACTTGTTGCTGTCTTAATGGAATGGTTTTC TACAGGAGCTGTAACATACTTAAAAATATGAATGTATTATGTAAATATGGCTTCTTTACATAAAAAATA AAATGTCAACACTGTACTTTTCTGAACACA 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_006796.3 |
Synonyms | OPA12; SCA28; SPAX5 |
Summary | This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008] |
Locus ID | 10939 |
MW | 24.2 |
Citations (1)
The use of this cDNA Clones has been cited in the following citations: |
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Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation
,null,
Journal of Medical Genetics
,PubMed ID 30910913
[AFG3L2]
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