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



Need custom modification / cloning service?
Get a free quote

CNY 4,845.00


货期*
3周

规格
    • 10 ug

Cited in 1 publication.

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

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
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Citations (1)

Documents

Customer Reviews 
Loading...