我们所展示的质粒图谱主要是从文献和开放数据库中收集而来,主要是为了方便研究工作,其中一小部分质粒进行了质量控制,可供科学家使用。
所有的产品都严格仅供科学研究使用,不能应用于临床试验,包括人体摄入、注射或外用的药理学用途。
确保质粒的关键元件正确,但是我们并不能保证实验结果。页面展示的图谱序列为理论序列,可能与测序结果不一致,请自行比对后确定是否满足要求。(如果测过序,本页面一般会提供下载)
开放数据库中的大多数载体序列都没有被完全测序。如果实际序列与参考序列的相似度超过99%,则将其视为正确。
由于科学研究是在探索未知,具有很大的不确定性,在任何情况下,我们都不承担超出质粒本身的额外经济损失或责任。
Yeast three-hybrid vector for expressing a "bait" protein fused to the GAL4 DNA-binding domain, plus an additional bridge protein.
- 载体名称:
- pBridge
- 载体抗性:
- Ampicillin
- 载体长度:
- 6527 bp
- 载体类型:
- Yeast Plasmids
- 复制子:
- ori
- 载体来源:
- Clontech
- 拷贝数:
- High copy number
- 启动子:
- ADH1
- 感受态:
- JM108
- 培养温度:
- 37℃
pBridge 载体图谱
质粒操作方法
1. 发货形式:质粒干粉(常温运输,存于-20度,请务必先转化提质粒后使用)
2. 收到质粒干粉后请先5000rpm离心1min,再加入20μl ddH2O溶解质粒;(质粒复测的浓度有时候与标称值差距较大,这可能是因为冻干质粒在管中的位置、复溶效率、测量偏差以及管壁的吸附导致,因此建议先转化提质粒后再使用)
3. 取1支100μl 感受态于冰上解冻10min,加入2μl质粒,再冰浴30min后,42℃热激60s,不要搅动,再冰浴2min;
4. 加入900μl无抗的LB液体培养基,180rpm震荡37℃培养45min (30℃培养1-1.5小时);
5. 6000rpm离心5min,仅留100μl上清液重悬细菌沉淀,并涂布至目标质粒抗性的LB平板上;
6. 将平板倒置37℃培养14h,如果要求是30℃则培养20h; (菌落过多则将质粒稀释后再转化;没有菌落则加入10μl质粒转化;建议不要直接转表达感受态, 要先转克隆感受态,重提质粒后再导入表达感受态);
7. 挑取单菌落至LB液体培养基中,加入对应抗生素,220rpm震荡培养14h,根据实验需要和质粒提取试剂盒说明书提取质粒。
pBridge 载体序列
LOCUS pBridge. 6527 bp DNA circular SYN 01-JAN-1980
DEFINITION Yeast three-hybrid vector for expressing a """"bait"""" protein
fused to the GAL4 DNA-binding domain, plus an additional bridge
protein.
ACCESSION .
VERSION .
KEYWORDS pBridge
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 6527)
AUTHORS Clontech
TITLE Direct Submission
REFERENCE 2 (bases 1 to 6527)
AUTHORS .
TITLE Direct Submission
COMMENT SGRef: number: 1; type: "Journal Article"
FEATURES Location/Qualifiers
source 1..6527
/mol_type="other DNA"
/organism="synthetic DNA construct"
promoter 10..406
/label=ADH1 promoter
/note="promoter for alcohol dehydrogenase 1"
CDS 434..874
/label=GAL4 DNA binding domain
/note="DNA binding domain of the GAL4 transcriptional
activator"
misc_feature 878..905
/label=MCS I
/note="MCS 1"
/note="multiple cloning site"
terminator 921..1108
/label=ADH1 terminator
/note="transcription terminator for the S. cerevisiae
alcohol dehydrogenase 1 (ADH1) gene"
CDS complement(1164..1835)
/label=TRP1
/note="phosphoribosylanthranilate isomerase, required for
tryptophan biosynthesis"
promoter complement(1836..1937)
/label=TRP1 promoter
primer_bind complement(1951..1967)
/label=M13 rev
/note="common sequencing primer, one of multiple similar
variants"
protein_bind complement(1975..1991)
/label=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(1999..2029)
/label=lac promoter
/note="promoter for the E. coli lac operon"
protein_bind complement(2044..2065)
/label=CAP binding site
/note="CAP binding activates transcription in the presence
of cAMP."
promoter 2259..2609
/label=MET17 promoter
/note="expression is repressed by methionine"
CDS 2619..2621
/codon_start=1
/product="start codon"
/label=start codon
/note="ATG"
/translation="M"
CDS 2631..2657
/label=HA
/note="HA (human influenza hemagglutinin) epitope tag"
CDS 2679..2699
/label=SV40 NLS
/note="nuclear localization signal of SV40 (simian virus
40) large T antigen"
misc_feature 2700..2723
/label=MCS II
/note="MCS 2"
/note="multiple cloning site"
terminator 2825..3095
/label=PGK1 terminator
/note="transcription terminator for 3-phosphoglycerate
kinase gene"
rep_origin complement(3357..3945)
/direction=LEFT
/label=ori
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
CDS complement(4119..4976)
/label=AmpR
/note="beta-lactamase"
promoter complement(4977..5081)
/label=AmpR promoter
rep_origin 5363..6527
/label=2u ori
/note="yeast 2u plasmid origin of replication"