久久久久国产成人精品亚洲午夜,成人免费毛片一区二区三区,国产成人久久精品激情91,国产成人无码精品久久久免费,精品欧美国产一区二区三区不卡,国产成人一区二区三区影院,国产精品久久久久久,久久久WWW成人免费精品,欧美91精品久久久久网免费

Size (kb): 6.8000001907348630

Vector: pIIIEx316 RPR (plasmid)

Promoters: Promoter for in vitro transcription T7

Construction: pRS316

Marker(s):URA3,ampR

Construct size (kb): 6.800000190734863

Features: insert detection: lacZ'
marker(s): URA3
marker(s): ampR
promoter: RPR1
promoter: lac
promoter for in vitro transcription: T3
promoter for in vitro transcription: T7
replicon: ARSH4
replicon: f1
replicon: pMB1
restriction site: BamHI
restriction site: EcoRI
restriction site: SalI
terminator: RPR1
centromere: CEN6

YC-type (centromeric) shuttle vector

vector permitting RNA synthesis in vitro

vector permitting expression of small structured RNAs

vector permitting production of single-stranded DNA

vector permitting visual detection of recombinants

vector with low copy number

Restriction digests of the clone give the following sizes (kb): EcoRI--6.8; BamHI--6.8; HindIII--6.8.

Cloned inserts can be transcribed from the S. cerevisiae RNase P RNA gene (RPR1) intragenic promoter to produce RPR1 leaders fused to RNA corresponding to inserted sequences.

One of a series of shuttle vectors (ATCC 87167 - 87182) designed for stable expression of small structured RNAs in yeast. The vectors differ in promoter/terminator cassettes, selectable markers, replicons, and copy number.

Constructed by insertion of a promoter/terminator cassette into the multiple cloning site of the shuttle vector pRS316.

Temperature: 37.0°C