pXB300 载体 (V002054)

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。

载体名称:
pXB300
载体抗性:
Tetracycline
载体长度:
4697 bp
载体类型:
Expression vector
复制子:
ori
载体来源:
Bina XR, Wong EA, Bina TF, Bina JE.
启动子:
tetR/tetAs

pXB300 载体载体图谱

pXB3004697 bp600120018002400300036004200TetRtetR/tetA promotersSK primerrrnB T1 terminatorrrnB T2 terminatorAmpR promoterAmpRf1 orioribomsokhok

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。

pXB300 载体载体序列

LOCUS       40924_47118        4697 bp DNA     circular SYN 18-DEC-2018
DEFINITION  Expression vector pXB300, complete sequence.
ACCESSION   .
VERSION     .
KEYWORDS    .
SOURCE      synthetic DNA construct
  ORGANISM  synthetic DNA construct
REFERENCE   1  (bases 1 to 4697)
  AUTHORS   Bina XR, Wong EA, Bina TF, Bina JE.
  TITLE     Construction of a tetracycline inducible expression vector and 
            characterization of its use in Vibrio cholerae
  JOURNAL   Plasmid 76C, 87-94 (2014)
  PUBMED    25451701
REFERENCE   2  (bases 1 to 4697)
  AUTHORS   Bina JE.
  TITLE     Direct Submission
  JOURNAL   Submitted (23-OCT-2014) Microbiology and Molecular Genetics, 
            University of Pittsburgh School of Medicine, 450 Technology Drive, 
            Pittsburgh, PA 15219, USA
REFERENCE   3  (bases 1 to 4697)
  TITLE     Direct Submission
REFERENCE   4  (bases 1 to 4697)
  AUTHORS   .
  TITLE     Direct Submission
COMMENT     SGRef: number: 1; type: "Journal Article"; journalName: "Plasmid 
            76C, 87-94 (2014)"
COMMENT     SGRef: number: 2; type: "Journal Article"; journalName: "Submitted 
            (23-OCT-2014) Microbiology and Molecular Genetics, University of 
            Pittsburgh School of Medicine, 450 Technology Drive, Pittsburgh, PA 
            15219, USA"
COMMENT     SGRef: number: 3; type: "Journal Article"
FEATURES             Location/Qualifiers
     source          1..4697
                     /mol_type="other DNA"
                     /organism="synthetic DNA construct"
     CDS             complement(29..652)
                     /codon_start=1
                     /label=TetR
                     /note="tetracycline repressor TetR"
                     /translation="MMSRLDKSKVINSALELLNEVGIEGLKTRKLAQKLGVEQPTLYWH
                     VKNKRALLDALAIEMLDRHHTHFCPLEGESWQDFLRNNAKSFRCALLSHRDGAKVHLGT
                     RPTEKQYETLENQLAFLCQQGFSLENALYALSAVGHFTLGCVLEDQEHQVAKEERETPT
                     TDSMPALLRQAIELFEHQGAEPAFLFGLELIICGLEKQLKCESGS"
     promoter        668..723
                     /label=tetR/tetA promoters
                     /note="overlapping promoters for bacterial tetR and tetA"
     primer_bind     759..775
                     /label=SK primer
                     /note="common sequencing primer, one of multiple similar 
                     variants"
     terminator      1042..1128
                     /label=rrnB T1 terminator
                     /note="transcription terminator T1 from the E. coli rrnB
                     gene"
     terminator      1220..1247
                     /label=rrnB T2 terminator
                     /note="transcription terminator T2 from the E. coli rrnB
                     gene"
     promoter        1266..1357
                     /label=AmpR promoter
     CDS             1358..2215
                     /codon_start=1
                     /label=AmpR
                     /note="beta-lactamase"
                     /translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI
                     ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRVDAGQEQLGRRIHYSQNDLVEYS
                     PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW
                     EPELNEAIPNDERDTTMPAAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA
                     LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS
                     LIKHW"
     rep_origin      2260..2715
                     /label=f1 ori
                     /note="f1 bacteriophage origin of replication; arrow
                     indicates direction of (+) strand synthesis"
     rep_origin      2826..3414
                     /label=ori
                     /note="high-copy-number ColE1/pMB1/pBR322/pUC origin of 
                     replication"
     misc_feature    complement(3600..3740)
                     /label=bom
                     /note="basis of mobility region from pBR322"
     CDS             complement(4131..4355)
                     /codon_start=1
                     /gene="sok"
                     /product="plasmid addiction system protein"
                     /label=sok
                     /protein_id="AJA39865.1"
                     /translation="MWTRHRDASWWLMKINLLRGYLLSATQHGNKPPSRHEAESLKRRA
                     HHSPYTCTLTTLTFPENNPLIQTVHGKSV"
     gene            complement(4131..4355)
                     /gene="sok"
                     /label=sok
     CDS             4399..4557
                     /codon_start=1
                     /gene="hok"
                     /product="plasmid addiction system protein"
                     /label=hok
                     /protein_id="AJA39864.1"
                     /translation="MKLPRSSLVWCVLIVCLTLLIFTYLTRKSLCEIRYRDGHREVAAF
                     MAYESGK"
     gene            4399..4557
                     /gene="hok"
                     /label=hok