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pACGFP1-N1质粒

货号：kl-zl-1061-01

货号	产品名称	规格	库存	价格	数量	购买
kl-zl-1061-01	pACGFP1-N1质粒	NA		立即咨询	+ -

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pACGFP1-N1质粒货号：kl-zl-1061 规格：20ul

启动子：	CMV promoter
复制子：	pUC ori,f1 ori
终止子：	SV40 poly(A) signal
质粒分类：	哺乳系列质粒；哺乳荧光质粒；哺乳绿色质粒
质粒大小：	4726bp
质粒标签：	C-GFP
原核抗性：	卡那霉素Kan（50μg/ml）
筛选标记：	新霉素Neo/G418
克隆菌株：	DH5α等大肠杆菌
培养条件：	37℃，有氧 LB
表达宿主：	293T等哺乳细胞
诱导方式：	无须诱导，瞬时表达
5'测序引物：	CMV-F（CGCAAATGGGCGGTAGGCGTG）
3'测序引物：	Sv40-polyA-R (GAAATTTGTGATGCTATTGC)

质粒简介：
pAcGFP1-N1质粒是 AcGFP的衍生物，来自Aequorea coerulescens。 AcGFP1已经优化了更亮的荧光。（激发最大值= 475nm;发射最大值= 505nm）AcGFP1基因的编码序列含有沉默碱基变化，其对应于人类密码子使用偏好。
pAcGFP1-N1 encodes a green fluorescent protein (GFP) from Aequorea coerulescens (excitationmaximum = 475 nm; emission maximum = 505 nm). The coding sequence of the AcGFP1 gene
contains silent base changes, which correspond to human codon-usage preferences (1). The MCSin pAcGFP1-N1 is between the immediate early promoter of CMV (PCMV IE) and the AcGFP1 coding
sequences. Genes cloned into the MCS will be expressed as fusions to the N-terminus of AcGFP1if they are in the same reading frame as AcGFP1 and there are no intervening stop codons. SV40
polyadenylation signals downstream of the AcGFP1 gene direct proper processing of the 3' end oftheAcGFP1 mRNA. The vector backbone also contains an SV40 origin for replication in mammalian
cells expressing the SV40 T antigen.Aneomycin-resistance cassette (Neor), consisting of the SV40earlypromoter,theneomycin/kanamycinresistancegeneofTn5,andpolyadenylationsignals fromthe
Herpes simplex virus thymidine kinase (HSV TK) gene, allows stably transfected eukaryotic cells tobe selected using G418.Abacterial promoter upstream of the gene expresses kanamycin resistance
in E. coli. The pAcGFP1-N1 backbone also provides a pUC origin of replication for propagation inE. coli and an f1 origin for single-stranded DNA production.
Fusions to the N terminus of AcGFP1 retain the fluorescent properties of the native protein allowingthe localization of the fusion protein in vivo . The target gene should be cloned into pAcGFP1-N1
so that it is in frame with the AcGFP1 coding sequences, with no intervening in-frame stop codons.The inserted gene should include the initiating ATG codon. The recombinant AcGFP1 vector can
be transfected into mammalian cells using any standard transfection method. If required, stabletransformants can be selected using G418 (2). pAcGFP1-N1 can also be used simply to express
AcGFP1 in a cell line of interest (e.g., as a transfection marker).
• Human cytomegalovirus (CMV) immediate early promoter： 1–589
Enhancer region：59–465; TATA box： 554–560
Transcription start point： 583
C→G mutation to remove Sac I site： 569
• Multiple Cloning Site (MCS)： 591–671
• Aequorea coerulescens Green Fluorescent Protein (AcGFP)： 673–1389
Start codon (ATG)： 673–675; Stop codon： 1390–1392
Insertion of Val at position 2： 676–678
Las amino acid： 1387–1389
• SV40 early mRNA polyadenylation signal
Polyadenylation signals： 1545–1550 & 1574–1579; mRNA 3' ends： 1583 & 1595
• f1 single-strand DNA origin： 1642–2097 (Packages the noncoding strand of AcGFP)
• Bacterial promoter for expression of Kanr gene：
–35 region： 2159–2164; –10 region： 2159–2164
Transcription start point： 2154
• SV40 origin of replication： 2438–2573
• SV40 early promoter
Enhancer (72-bp tandem repeats)： 2271–2342 & 2343–2414
21-bp repeats： 2418–2438, 2439–2459 & 2467–2481
Early promoter element： 2494–2500
Major transcription start points： 2490, 2528, 2534 & 2539
• Kanamycin/neomycin resistance gene：
Neomycin phosphotransferase coding sequences： start codon (ATG)： 2622–2624; stop codon： 3414–3416
GA mutation to remove Pst I site： 2804
C-A (Arg to Ser) mutation to remove BssHII site： 3150
• Herpes simplex virus (HSV) thymidine kinase (TK) polyadenylation signal
Polyadenylation signals： 3652–3657 & 3665–3670
• pUC plasmid replication origin： 4001–4644
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