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-43.1b
- 库存:
100
- 供应商:
LSMBIO
- 规格:
2ug
pET-43.1b
Search name
pET-43.1b,Plasmid pET-43.1b,pET-43.1b vector
pET-43.1b information
Promoter: T7/lac
Replicator: ColE1 ori, F1 ori
Terminator: T7 Terminator
Plasmid classification: Escherichia coli vector; PET series expression plasmid
Plasmid size: 7274bp
Plasmid Tags: C-HSV, N-6 x His, C-6 x His, N-Thrombin, N-Nus, N-EK
Prokaryotic resistance: ampicillin Amp
Cloned strain: DH5 alpha
Culture conditions: 37 centigrade, aerobic, LB
Expression host: BL21 (DE3)
Culture conditions: 37 centigrade, aerobic, LB
Inducement: IPTG or lactose and its analogues
5'sequencing primers: T7:TAATACGACTCACTATAGGG
3'sequencing primers: T7-ter:TGCTAGTTATTGCTCAGCGG
pET-43.1b Description
pET-43.1 series of vectors are designed for cloning and high-level expression of peptide sequences fused with the 491 aa Nus•Tag™ protein. 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 circle 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 ColiDOWN primer. Vector encoded sequence can be completely removed when cloning into the PshA I or Sma I sites (as shown below) by cleaving the Nus•Tag fusion protein with enterokinase or thrombin, respectively.
pET-43.1b Sequence
LOCUS Exported 7274 bp ds-DNA circular SYN 10-8-2015
DEFINITION synthetic circular DNA
ACCESSION .
VERSION .
KEYWORDS Untitled 6
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 7274)
AUTHORS .
TITLE Direct Submission
JOURNAL Exported 2015-8-10 from MLCC
FEATURES Location/Qualifiers
source 1..7274
/organism="synthetic DNA construct"
/mol_type="other DNA"
source 2325..2347
/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"
terminator 141..168
/note="rrnB T2 terminator"
/note="transcription terminator T2 from the E. coli rrnB
gene"
terminator 260..346
/gene="Escherichia coli rrnB"
/note="rrnB T1 terminator"
/note="transcription terminator T1 from the E. coli rrnB
gene"
CDS complement(512..529)
/codon_start=1
/product="6xHis affinity tag"
/note="6xHis"
/translation="HHHHHH"
CDS complement(536..568)
/codon_start=1
/product="HSV (herpes simplex virus) epitope tag"
/note="HSV tag"
/translation="QPELAPEDPED"
CDS complement(680..694)
/codon_start=1
/product="enterokinase recognition and cleavage site"
/note="enterokinase site"
/translation="DDDDK"
CDS complement(713..730)
/codon_start=1
/product="thrombin recognition and cleavage site"
/note="thrombin site"
/translation="LVPRGS"
CDS complement(746..790)
/codon_start=1
/product="affinity and epitope tag derived from pancreatic
ribonuclease A"
/note="S-Tag"
/translation="KETAAAKFERQHMDS"
CDS complement(800..817)
/codon_start=1
/product="6xHis affinity tag"
/note="6xHis"
/translation="HHHHHH"
CDS complement(833..2317)
/codon_start=1
/gene="nusA"
/product="transcription elongation protein (N utilization
substance protein A)"
/note="NusA"
/note="highly soluble in E. coli"
/translation="MNKEILAVVEAVSNEKALPREKIFEALESALATATKKKYEQEIDV
RVQIDRKSGDFDTFRRWLVVDEVTQPTKEITLEAARYEDESLNLGDYVEDQIESVTFDR
ITTQTAKQVIVQKVREAERAMVVDQFREHEGEIITGVVKKVNRDNISLDLGNNAEAVIL
REDMLPRENFRPGDRVRGVLYSVRPEARGAQLFVTRSKPEMLIELFRIEVPEIGEEVIE
IKAAARDPGSRAKIAVKTNDKRIDPVGACVGMRGARVQAVSTELGGERIDIVLWDDNPA
QFVINAMAPADVASIVVDEDKHTMDIAVEAGNLAQAIGRNGQNVRLASQLSGWELNVMT
VDDLQAKHQAEAHAAIDTFTKYLDIDEDFATVLVEEGFSTLEELAYVPMKELLEIEGLD
EPTVEALRERAKNALATIAQAQEESLGDNKPADDLLNLEGVDRDLAFKLAARGVCTLED
LAEQGIDDLADIEGLTDEKAGALIMAARNICWFGDEA"
RBS 2325..2347
/note="efficient ribosome binding site from bacteriophage
T7 gene 10 (Olins and Rangwala, 1989)"
protein_bind 2362..2386
/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(2387..2405)
/note="T7 promoter"
/note="promoter for bacteriophage T7 RNA polymerase"
promoter 2718..2795
/gene="lacI"
/note="lacI promoter"
CDS 2796..3878
/codon_start=1
/gene="lacI"
&n <
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PET39b PET40b PET41a PET42a PET42b PET43.1b PET44a PET48b PET50b PET52b
很多新手在问做原核表达需要考虑的载体和菌株的选择,现系统地解答一下,供新手借鉴。
片段,而不需要限制性消化载体或插入片段。 溶解性和细胞定位 考虑了目标蛋白的应用和克隆策略,还应该确定目标蛋白的细胞定位和溶解性,这一点十分重要。在许多实际应用中常希望表达可溶的活性蛋白。 特定目标蛋白的溶解性取决于多种因素,包括各自的蛋白序列。在许多情况下,溶解性不是有或无的现象,载体、宿主菌和培养条件可被用来增加或减少获得的可溶或不可溶形式的比例。 PET-32 载体系列使目标序列与通常能够增加可溶性蛋白比例的硫氧还蛋白 (Trx.Tag ) 融合。新推出的 pET-43.1 系列具有
溶解性和细胞定位 考虑了目标蛋白的应用和克隆策略,还应该确定目标蛋白的细胞定位和溶解性,这一点十分重要。在许多实际应用中常希望表达可溶的活性蛋白。 特定目标蛋白的溶解性取决于多种因素,包括各自的蛋白序列。在许多情况下,溶解性不是有或无的现象,载体、宿主菌和培养条件可被用来增加或减少获得的可溶或不可溶形式的比例。 PET-32 载体系列使目标序列与通常能够增加可溶性蛋白比例的硫氧还蛋白 (Trx.Tag ) 融合。新推出的 pET-43.1 系列具有通过大量系统筛选而得到
技术资料暂无技术资料 索取技术资料










