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度
- 保质期:
2年
- 供应商:
钦诚生物
- 规格:
5ug
基本信息
| 启动子: | PC,polyhedrin |
|---|---|
| 复制子: | pUC ori,F1 ori |
| 终止子: | SV40 poly(A) signal |
| 质粒分类: | 广宿主系列,昆虫细胞载体 |
| 质粒大小: | 4857bp |
| 质粒标签: | N-His;N-TEV |
| 原核抗性: | Amp |
| 筛选标记: | Gen |
| 克隆菌株: | DH5α |
| 培养条件: | 37℃,有氧 LB |
| 表达宿主: | 昆虫细胞 |
| 诱导方式: | 无须诱导,瞬时表达 |
| 5'测序引物: | pFastbac-F: TATTCCGGATTATTCATACC |
| 3'测序引物: | pFastBac-R: ACAAATGTGGTATGGCTGA |
质粒简介
The pFastBac HT vector is supplied with the multiple cloning site in three reading frames (A, B, and C) to facilitate cloning your gene of interest in frame with the N-terminal 6xHis tag
质粒图谱
质粒序列
LOCUS Exported 4857 bp ds-DNA circular SYN 09-SEP-2016
DEFINITION synthetic circular DNA
ACCESSION .
VERSION .
KEYWORDS Untitled
SOURCE synthetic DNA construct
ORGANISM synthetic DNA construct
REFERENCE 1 (bases 1 to 4857)
AUTHORS .
TITLE Direct Submission
JOURNAL Exported Friday, September 9, 2016 from SnapGene Viewer 3.1.4
FEATURES Location/Qualifiers
source 1..4857
/organism="synthetic DNA construct"
/mol_type="other DNA"
rep_origin 2..457
/direction=RIGHT
/note="f1 ori"
/note="f1 bacteriophage origin of replication; arrow
indicates direction of (+) strand synthesis"
promoter 484..588
/gene="bla"
/note="AmpR promoter"
CDS 589..1449
/codon_start=1
/gene="bla"
/product="beta-lactamase"
/note="AmpR"
/note="confers resistance to ampicillin, carbenicillin, and
related antibiotics"
/translation="MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYI
ELDLNSGKILESFRPEERFPMMSTFKVLLCGAVLSRIDAGQEQLGRRIHYSQNDLVEYS
PVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRW
EPELNEAIPNDERDTTMPVAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSA
LPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGAS
LIKHW"
rep_origin 1620..2208
/direction=RIGHT
/note="ori"
/note="high-copy-number ColE1/pMB1/pBR322/pUC origin of
replication"
mobile_element 2511..2735
/mobile_element_type="transposon:Tn7"
/note="Tn7R"
/note="mini-Tn7 element (right end of the Tn7 transposon)"
CDS complement(2802..3335)
/codon_start=1
/gene="aacC1"
/product="gentamycin acetyltransferase"
/note="GmR"
/note="confers resistance to gentamycin"
/translation="MLRSSNDVTQQGSRPKTKLGGSSMGIIRTCRLGPDQVKSMRAALD
LFGREFGDVATYSQHQPDSDYLGNLLRSKTFIALAAFDQEAVVGALAAYVLPRFEQPRS
EIYIYDLAVSGEHRRQGIATALINLLKHEANALGAYVIYVQADYGDDPAVALYTKLGIR
EEVMHFDIDPSTAT"
promoter complement(3524..3552)
/gene="intI1 (promoter lies within the coding sequence)"
/note="Pc promoter"
/note="class 1 integron promoter"
promoter 3904..3995
/gene="polh from Autographa californica"
/note="polyhedrin promoter"
/note="promoter for the baculovirus polyhedrin gene"
CDS 4062..4079
/codon_start=1
/product="6xHis affinity tag"
/note="6xHis"
/translation="HHHHHH"
CDS 4101..4121
/codon_start=1
/product="tobacco etch virus (TEV) protease recognition and
cleavage site"
/note="TEV site"
/translation="ENLYFQG"
polyA_signal 4347..4481
/note="SV40 poly(A) signal"
/note="SV40 polyadenylation signal"
mobile_element 4510..4675
/mobile_element_type="transposon:Tn7"
/note="Tn7L"
/note="mini-Tn7 element (left end of the Tn7 transposon)"
ORIGIN
1 gacgcgccct gtagcggcgc attaagcgcg gcgggtgtgg tggttacgcg cagcgtgacc
61 gctacacttg ccagcgccct agcgcccgct cctttcgctt tcttcccttc ctttctcgcc
121 acgttcgccg gctttccccg tcaagctcta aatcgggggc tccctttagg gttccgattt
181 agtgctttac ggcacctcga ccccaaaaaa cttgattagg gtgatggttc acgtagtggg
241 ccatcgccct gatagacggt ttttcgccct ttgacgttgg agtccacgtt ctttaatagt
301 ggactcttgt tccaaactgg aacaacactc aaccctatct cggtctattc ttttgattta
361 taagggattt tgccgatttc ggcctattgg ttaaaaaatg agctgattta acaaaaattt
421 aacgcgaatt ttaacaaaat attaacgttt acaatttcag gtggcacttt tcggggaaat
481 gtgcgcggaa cccctatttg tttatttttc taaatacatt caaatatgta tccgctcatg
541 agacaataac cctgataaat gcttcaataa tattgaaaaa ggaagagtat gagtattcaa
601 catttccgtg tcgcccttat tccctttttt gcggcatttt gccttcctgt ttttgctcac
661 ccagaaacgc tggtgaaagt aaaagatgct gaagatcagt tgggtgcacg agtgggttac
721 atcgaactgg atctcaacag cggtaagatc cttgagagtt ttcgccccga agaacgtttt
781 ccaatgatga gcacttttaa agttctgcta tgtggcgcgg tattatcccg tattgacgcc
841 gggcaagagc aactcggtcg ccgcatacac tattctcaga atgacttggt tgagtactca
901 ccagtcacag aaaagcatct tacggatggc atgacagtaa gagaattatg cagtgctgcc
961 ataaccatga gtgataacac tgcggccaac ttacttctga caacgatcgg aggaccgaag
1021 gagctaaccg cttttttgca caacatgggg gatcatgtaa ctcgccttga tcgttgggaa
1081 ccggagctga atgaagccat accaaacgac gagcgtgaca ccacgatgcc tgtagcaatg
1141 gcaacaacgt tgcgcaaact attaactggc gaactactta ctctagcttc ccggcaacaa
1201 ttaatagact ggatggaggc ggataaagtt gcaggaccac ttctgcgctc ggcccttccg
1261 gctggctggt ttattgctga taaatctgga gccggtgagc gtgggtctcg cggtatcatt
1321 gcagcactgg ggccagatgg taagccctcc cgtatcgtag ttatctacac gacggggagt
1381 caggcaacta tggatgaacg aaatagacag atcgctgaga taggtgcctc actgattaag
1441 cattggtaac tgtcagacca agtttactca tatatacttt agattgattt aaaacttcat
1501 ttttaattta aaaggatcta ggtgaagatc ctttttgata atctcatgac caaaatccct
1561 taacgtgagt tttcgttcca ctgagcgtca gaccccgtag aaaagatcaa aggatcttct
1621 tgagatcctt tttttctgcg cgtaatctgc tgcttgcaaa caaaaaaacc accgctacca
1681 gcggtggttt gtttgccgga tcaagagcta ccaactcttt ttccgaaggt aactggcttc
1741 agcagagcgc agataccaaa tactgtcctt ctagtgtagc cgtagttagg ccaccacttc
1801 aagaactctg tagcaccgcc tacatacctc gctctgctaa tcctgttacc agtggctgct
1861 gccagtggcg ataagtcgtg tcttaccggg ttggactcaa gacgatagtt accggataag
1921 gcgcagcggt cgggctgaac ggggggttcg tgcacacagc ccagcttgga gcgaacgacc
1981 tacaccgaac tgagatacct acagcgtgag cattgagaaa gcgccacgct tcccgaaggg
2041 agaaaggcgg acaggtatcc ggtaagcggc agggtcggaa caggagagcg cacgagggag
2101 cttccagggg gaaacgcctg gtatctttat agtcctgtcg ggtttcgcca cctctgactt
2161 gagcgtcgat ttttgtgatg ctcgtcaggg gggcggagcc tatggaaaaa cgccagcaac
2221 gcggcctttt tacggttcct ggccttttgc tggccttttg ctcacatgtt ctttcctgcg
2281 ttatcccctg attctgtgga taaccgtatt accgcctttg agtgagctga taccgctcgc
2341 cgcagccgaa cgaccgagcg cagcgagtca gtgagcgagg aagcggaaga gcgcctgatg
2401 cggtattttc tccttacgca tctgtgcggt atttcacacc gcagaccagc cgcgtaacct
2461 ggcaaaatcg gttacggttg agtaataaat ggatgccctg cgtaagcggg tgtgggcgga
2521 caataaagtc ttaaactgaa caaaatagat ctaaactatg acaataaagt cttaaactag
2581 acagaatagt tgtaaactga aatcagtcca gttatgctgt gaaaaagcat actggacttt
2641 tgttatggct aaagcaaact cttcattttc tgaagtgcaa attgcccgtc gtattaaaga
2701 ggggcgtggc caagggcatg gtaaagacta tattcgcggc gttgtgacaa tttaccgaac
2761 aactccgcgg ccgggaagcc gatctcggct tgaacgaatt gttaggtggc ggtacttggg
2821 tcgatatcaa agtgcatcac ttcttcccgt atgcccaact ttgtatagag agccactgcg
2881 ggatcgtcac cgtaatctgc ttgcacgtag atcacataag caccaagcgc gttggcctca
2941 tgcttgagga gattgatgag cgcggtggca atgccctgcc tccggtgctc gccggagact
3001 gcgagatcat agatatagat ctcactacgc ggctgctcaa acctgggcag aacgtaagcc
3061 gcgagagcgc caacaaccgc ttcttggtcg aaggcagcaa gcgcgatgaa tgtcttacta
3121 cggagcaagt tcccgaggta atcggagtcc ggctgatgtt gggagtaggt ggctacgtct
3181 ccgaactcac gaccgaaaag atcaagagca gcccgcatgg atttgacttg gtcagggccg
3241 agcctacatg tgcgaatgat gcccatactt gagccaccta actttgtttt agggcgactg
3301 ccctgctgcg taacatcgtt gctgctgcgt aacatcgttg ctgctccata acatcaaaca
3361 tcgacccacg gcgtaacgcg cttgctgctt ggatgcccga ggcatagact gtacaaaaaa
3421 acagtcataa caagccatga aaaccgccac tgcgccgtta ccaccgctgc gttcggtcaa
3481 ggttctggac cagttgcgtg agcgcatacg ctacttgcat tacagtttac gaaccgaaca
3541 ggcttatgtc aactgggttc gtgccttcat ccgtttccac ggtgtgcgtc acccggcaac
3601 cttgggcagc agcgaagtcg aggcatttct gtcctggctg gcgaacgagc gcaaggtttc
3661 ggtctccacg catcgtcagg cattggcggc cttgctgttc ttctacggca aggtgctgtg
3721 cacggatctg ccctggcttc aggagatcgg aagacctcgg ccgtcgcggc gcttgccggt
3781 ggtgctgacc ccggatgaag tggttcgcat cctcggtttt ctggaaggcg agcatcgttt
3841 gttcgcccag gactctagct atagttctag tggttggcta cgtatactcc ggaatattaa
3901 tagatcatgg agataattaa aatgataacc atctcgcaaa taaataagta ttttactgtt
3961 ttcgtaacag ttttgtaata aaaaaaccta taaatattcc ggattattca taccgtccca
4021 ccatcgggcg cggatctcgg tccgaaacca tgtcgtacta ccatcaccat caccatcacg
4081 attacgatat cccaacgacc gaaaacctgt attttcaggg cgccatggga tccggaattc
4141 aaaggcctac gtcgacgagc tcactagtcg cggccgcttt cgaatctaga gcctgcagtc
4201 tcgaggcatg cggtaccaag cttgtcgaga agtactagag gatcataatc agccatacca
4261 catttgtaga ggttttactt gctttaaaaa acctcccaca cctccccctg aacctgaaac
4321 ataaaatgaa tgcaattgtt gttgttaact tgtttattgc agcttataat ggttacaaat
4381 aaagcaatag catcacaaat ttcacaaata aagcattttt ttcactgcat tctagttgtg
4441 gtttgtccaa actcatcaat gtatcttatc atgtctggat ctgatcactg atatcgccta
4501 ggagatccga accagataag tgaaatctag ttccaaacta ttttgtcatt tttaattttc
4561 gtattagctt acgacgctac acccagttcc catctatttt gtcactcttc cctaaataat
4621 ccttaaaaac tccatttcca cccctcccag ttcccaacta ttttgtccgc ccacagcggg
4681 gcatttttct tcctgttatg tttttaatca aacatcctgc caactccatg tgacaaaccg
4741 tcatcttcgg ctactttttc tctgtcacag aatgaaaatt tttctgtcat ctcttcgtta
4801 ttaatgtttg taattgactg aatatcaacg cttatttgca gcctgaatgg cgaatgg
//
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-GFP 等)以及其他应用的质粒。根据质粒的拷贝数不同,又可以分为高拷贝质粒(质粒可以在细胞内复制成几百个拷贝)和低拷贝质粒(质粒在细胞内只有<20 个拷贝)。质粒的拷贝数通常受到复制子的调控。 质粒上通常会带有多种元件,例如,复制起始位点(ORI),抗性基因,多克隆位点,启动子,终止子,标签序列等等。质粒上至少要带有复制位点(ORI),否则无法进行复制;除了一些特殊质粒(如 minicircle plasmid)之外,绝大多数质粒都带有抗性基因,用于抗生素筛选。多克隆位点可以通过酶切,酶连或者同源
一. 植物遗传转化的方法 植物遗传转化技术可分为两大类:一类是直接基因转移技术,包括基因枪法、原生质体法、脂质体法、花粉管通道法、电激转化法、PEG介导转化方法等,其中基因枪转化法是代表。另一类是生物介导的转化方法,主要有农杆菌介导和病毒介导两种转化方法,其中农杆菌介导的转化方法操作简便、成本低、转化率高,广泛应用于双子叶植物的遗传转化。二.农杆菌介导的基因转化方法 (一)农杆菌的Ti质粒与T-DNA 的整合机制几乎所有双子叶植物都容易受到土壤农杆菌感染,而产生根瘤。它是一种革兰氏阴性土壤杆菌
转染的定义是“将具生物功能的核酸转移或运送到细胞内并使核酸在细胞内维持其生物功能”。其中,核酸包括DNA (质粒和线性双链DNA ),反义寡核苷酸及RNAi(RNA interference)。基因转染技术已广泛应用于基因组功能研究(基因表达调控,基因功能,信号转导和药物筛选研究)和基因治疗研究。基因转染需要一定的转染试剂将带有目的基因的载体运送到细胞内。早期的磷酸钙转染法转染效率很低,且对很多细胞株无效,因此不能满足很多科研工作的需要。目前,最常用的转染试剂是阳离子脂质体和阳离子聚合
技术资料暂无技术资料 索取技术资料




