相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
负20摄氏度
- 保质期:
3个月
- 英文名:
pET-30c
- 库存:
100
- 供应商:
LSMBIO
- 规格:
2ug
pET-30c
Search name
pET-30c,Plasmid pET-30c,pET-30c vector
pET-30c Information
Promoter: T7/lac
Replicon: ColE1 ori, F1 ori
Terminator: T7 Terminator
Plasmid classification: Escherichia coli vector; PET series expression plasmid
Plasmid size: 5423bp
Plasmid tagging: N-6 * His, N-S, N-Thrombin, N-EK, C-6 * His
Prokaryotic resistance: kanamycin Kan
Clonal strain: DH5 alpha
Culture conditions: 37 C, aerobic, LB
Expression host: BL21 (DE3)
Culture conditions: 37 C, aerobic, LB
Induction: IPTG or lactose and its analogues.
5'sequencing primers: T7:TAATACGACTCACTATAGGG
3'sequencing primers: T7-ter:TGCTAGTTATTGCTCAGCGG
pET-30c Description
The pET-30a-c(+) vectors carry an N-terminal His• Tag/ thrombin/ S• Tag/ enterokinase configuration plus an optional C-terminal His• Tag sequence. Unique sites are shown on the circle map. Note that the sequence is numbered by the pBR322 convention, so the T7 expression region is reversed on the circular map. The cloning/expression region of the coding strand transcribed by T7 RNA polymerase is shown below. The f1 origin is oriented so that infection with helper phage will produce virions containing single-stranded DNA that corresponds to the coding strand. Therefore, single-stranded sequencing should be performed using the T7 terminator primer .
pET-30c Multiple cloning site
pET-30c Sequence
LOCUS Exported 5423 bp ds-DNA circular SYN 05-8-2015
DEFINITION synthetic circular DNA
ACCESSION .
VERSION .
KEYWORDS Untitled 5
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 5423)
AUTHORS .
TITLE Direct Submission
JOURNAL Exported 2015-8-5
FEATURES Location/Qualifiers
source 1..5423
/organism="synthetic DNA construct"
/mol_type="other DNA"
source 356..378
/organism="Enterobacteria phage T7"
/mol_type="genomic DNA"
/db_xref="taxon:10760"
terminator 26..73
/note="T7 terminator"
/note="transcription terminator for bacteriophage T7 RNA
polymerase"
CDS complement(140..157)
/codon_start=1
/product="6xHis affinity tag"
/note="6xHis"
/translation="HHHHHH"
CDS complement(220..234)
/codon_start=1
/product="enterokinase recognition and cleavage site"
/note="enterokinase site"
/translation="DDDDK"
CDS complement(250..294)
/codon_start=1
/product="affinity and epitope tag derived from pancreatic
ribonuclease A"
/note="S-Tag"
/translation="KETAAAKFERQHMDS"
CDS complement(301..318)
/codon_start=1
/product="thrombin recognition and cleavage site"
/note="thrombin site"
/translation="LVPRGS"
CDS complement(328..345)
/codon_start=1
/product="6xHis affinity tag"
/note="6xHis"
/translation="HHHHHH"
RBS 356..378
/note="efficient ribosome binding site from bacteriophage
T7 gene 10 (Olins and Rangwala, 1989)"
protein_bind 393..417
/bound_moiety="lac repressor encoded by lacI"
/note="lac operator"
/note="The lac repressor binds to the lac operator to
inhibit transcription in E. coli. This inhibition can be
relieved by adding lactose or
isopropyl-beta-D-thiogalactopyranoside (IPTG)."
promoter complement(418..436)
/note="T7 promoter"
/note="promoter for bacteriophage T7 RNA polymerase"
promoter 749..826
/gene="lacI"
/note="lacI promoter"
CDS 827..1909
/codon_start=1
/gene="lacI"
/product="lac repressor"
/note="lacI"
/note="The lac repressor binds to the lac operator to
inhibit transcription in E. coli. This inhibition can be
relieved by adding lactose or
isopropyl-beta-D-thiogalactopyranoside (IPTG)."
/translation="MKPVTLYDVAEYAGVSYQTVSRVVNQASHVSAKTREKVEAAMAEL
NYIPNRVAQQLAGKQSLLIGVATSSLALHAPSQIVAAIKSRADQLGASVVVSMVERSGV
EACKAAVHNLLAQRVSGLIINYPLDDQDAIAVEAACTNVPALFLDVSDQTPINSIIFSH
EDGTRLGVEHLVALGHQQIALLAGPLSSVSARLRLAGWHKYLTRNQIQPIAEREGDWSA
MSGFQQTMQMLNEGIVPTAMLVANDQMALGAMRAITESGLRVGADISVVGYDDTEDSSC
YIPPLTTIKQDFRLLGQTSVDRLLQLSQGQAVKGNQLLPVSLVKRKTTLAPNTQTASPR
ALADSLMQLARQVSRLESGQ"
CDS 2718..2909
/codon_start=1
/gene="rop"
/product="Rop protein, which maintains plasmids at low copy
number"
/note="rop"
/translation="MTKQEKTALNMARFIRSQTLTLLEKLNELDADEQADICESLHDHA
DELYRSCLARFGDDGENL"
misc_feature 3011..3153
/note="bom"
/note="basis of mobility region from pBR322"
rep_origin complement(3339..3927)
/direction=LEFT
/note="ori"
<
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验DYCZ一28A、28B、28C、28D、29、30型夹芯式垂直电泳槽
一、组成部件(一)装有铂金丝的贮液槽一对,配有冷却装置及电泳缓冲液流出口。(二)凹型橡胶框,配有玻璃板,可分别制作厚度为lmm、1.5mm的凝胶板,操作时根据需要选择适当厚度的玻璃板及梳子配套使用。(三)样品孔模具(梳子)用于电泳加样。(四)固定贮液槽的螺丝杆及螺母4对,28D、30型为5对。(五)橡胶管五根。两根长的用于连接冷却水的出入口;中等长度的两根用于连接电极缓;中液的流出口;最短的一根用于连接贮液槽间的冷却水。(六)导线1付。二、使用方法(一)清洗部件上述部件组装前要彻底清洗干净
的BL-21 / pET32a(+)/ pTBO超声处理后的上清液; 泳道3:诱导BL-21 / pET 32a(+)/ pTBO超声处理后沉淀; 泳道4:BL-21 / pET 32a(+)/ pTBO超声处理诱导5小时后的上清液。pTBO融合蛋白的分子量约为22kDa。经验对于原核物种中的异源蛋白质表达,首先,我们需要优化通常用于大肠杆菌的密码子。其次,在培养基中加入IPTG后,让培养物生长不同的时间点,如3小时,6小时,12小时18小时,并在37°C,30°C,21°C或不同的温度下尝试不同
dmdfe 本人将GFP基因后面加了一段大约110bp的序列,插入PET28A的BamH1和Hind3位点,最后在BL21中表达。 经SDS-PAGE验证表明: 目的蛋白 大量存在菌体裂解后沉淀即包涵体中,但是该沉淀无色。 少量存在于上清中,上清显微弱的绿色。 看文献大量报道GFP融合蛋白几乎都形成可溶性表达,目的蛋白在上清中,并且诱导条件没有太大要求。 想请教一下各位做过GFP原核表达的经验
技术资料暂无技术资料 索取技术资料








