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product summary
company name :
Addgene
product type :
cDNA
product name :
pFA5
catalog :
46791
citations: 1
product information
Catalog Number :
46791
Product Name :
pFA5
article :
doi | 10.1371/journal.pone.0008111 |
id | 6956 |
pubmed_id | 19956593 |
bacterial resistance :
Ampicillin
cloning :
backbone | pYES2.1/V5-His/lacZ | |
backbone_mutation | The vector used for galactose-induced yeast expression of C-terminal double tagged (V5 and 6xHis) proteins was the pYES2.1/V5-His-TOPO (Invitrogen) and cloning was according to the manufacturer s specifications. The identity of the cloned material was confirmed by restriction digestion analysis and DNA sequencing. PFA1 contains the full-length wild-type Fun30 sequence. The coding region of Fun30, including the 2 codons immediately upstream of the sequence and excluding the stop codon were amplified by polymerase chain reaction (PCR) from purified genomic DNA using the enzyme PfuUltra (Stratagene) following the manufacturer s specifications. The primers used were: forward F30 (GTCGACGAAAACATGAGTGGTTCG) and reverse F30 (CTCGAGTTCTTTGGTTCCCTTCGG), which introduced a SalI and an XhoI restriction enzyme sites in the fragment amplified, in the 5 - and 3 - ends, respectively. 3 adenylation of the amplified fragments was done by PCR, after which the TOPO cloning reaction was performed. PFA5 contains a version of Fun30 without the Cue domain. From PFA1, a sequence containing the Cue domain was removed by restriction digestion with the enzymes Bsu36I and BclI. The remaining PFA1 was ligated to a sequence previously amplified from PFA1. This sequence was amplified using the primers removeCforward (TATATTCCTGAGGATAGGCAGCAA) and removeCreverse (GGAAGAACATTTCTTGATCACAGA) and cut with the restriction enzymes Bsu36I and BclI. The ligation was performed using the enzyme Quick T4 DNA Ligase (New England BioLabs). | |
backbone_origin | Invitrogen | |
backbone_size | 8964 | |
promoter | ||
sequencing_primer_3 | ||
sequencing_primer_5 | ||
vector_types |
|
growth strain :
To express a version of Fun30 without CUE domain in budding yeast
origin :
37
pi :
|
resistance markers :
1634 |
tags :
Unknown
terms :
URA3 |
company information
Addgene
490 Arsenal Way, Suite 100
Watertown, MA 02472
Watertown, MA 02472
info@addgene.org
https://www.addgene.org617.225.9000
headquarters: USA
questions and comments