Takara、Clontech、UElandy Inc(试剂)代理
Takara、Clontech、UElandy Inc(试剂)代理
简要描述:Clontech,代理,国内代理,上海代理,北京代理,中国代理,代理, PCR产品
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Clontech,Clontech代理,国内代理,上海代理,北京代理,中国代理,代理, PCR产品
Clontech 四环素调控系统 pRevTRE载体
型号 | 载体名称 | 出品公司 | 载体用途 |
VSC0468 | pRevTRE | Clontech | 四环素调控系统 |
Promotor: LTR
Size: 6500
Selectable Marker: Hygromycin
Constitutive: Inducible
Viral/Non-Viral: Retroviral
pRevTRE is a retroviral Tet response vector that expresses a gene of interest from the Tet-response element (TRE). This vector is derived from pLNCX, a retroviral vector created using elements of Moloney murine leukemia virus (MoMuLV) and Moloney murine sarcoma virus (MoMuSV) as described. The TRE contains seven direct repeats of the tetO operator sequence, upstream of a minimal CMV promoter, which can be bound by the tTA and rtTA transactivators. The 5′ viral LTR controls expression of the transcript that contains Y+ (the extended viral packaging signal) and the hygromycin resistance (Hygr) gene for antibiotic selection in mammalian cells. The TRE is derived from vectors described previously. pRevTRE also includes the E. coli Ampr gene for antibiotic selection in bacteria.
The complete RevTet-Off and RevTet-On Systems also include the control vector pRevTRE-Luc, which was constructed by cloning the firefly luciferase gene into the HindIII/Cla I sites in the MCS of pRevTRE.
Clontech AH109说明书,AH109说明书,Clontech AH109
型号 | 载体名称 | 出品公司 | 载体用途 |
VNC0491 | AH109 | Clontech | 配套酿酒酵母 |
his section provides detailed phenotypes of the yeast strains included with MATCHMAKER System 3
and MATCHMAKER GAL4 cDNA and Genomic Libraries. For additional information on the growth and
maintenance of yeast, see the YPH, Chapter III. We also recommend Guthrie & Fink’s Guide to Yeast
Genetics and Molecular Biology (1991) and Heslot & Gailardin’s Molecular Biology and Genetic
Engineering of Yeasts (1992).
A. Yeast Host Strains
The complete genotypes of AH109, Y187, and CG-1945 are provided in Table II. All strains are
gal4
–
and gal80
–
; this prevents interference of native regulatory proteins with the regulatory
elements in the two-hybrid system.
1. Use AH109 as the host strain if you plan to screen an AD/library using HIS3, ADE2, and MEL1.
2. System 3 Users Only: Use Y187 as the host strain if you plan to test for an interaction between
two known proteins using the lacZ reporter only. In addition, use Y187 as a mating partner to
verify protein interactions.
3. Library Users Only: Use CG-1945 as the host strain if you plan to separate DNA/bait and
AD/library plasmids by cycloheximide counterselection. Alternatively, use pGBKT7 to construct your bait. This DNA-BD vector contains a kanamycin resistance marker; therefore,
vectors can be separated in E. coli without cycloheximide counterselection.
Clontech 酵母双杂交系统 pGBKT7, 酵母双杂交系统 pGBKT7,Clontech pGBKT7
Mammalian Selection:TRP1 (HIS3 selection)
Clontech pBridge酵母三杂交系统说明书
载体描述:
pBridge expresses two proteins: a DNA-binding domain fusion, and an additional protein. pBridge thus allows establishment of three-hybrid systems when used in combination with an activation domain fusion vector and yeast strains from any of Clontech’s GAL4-based two-hybrid systems, including Matchmaker™ Gold. This vector generates a hybrid protein that contains the sequences for the GAL4 DNA-binding domain (DNA-BD) and the sequence cloned into MCS I. The fusion protein is expressed in yeast host cells from the constitutive ADH1 promoter; transcription is terminated at the ADH1 transcription termination signal. The hybrid protein is targeted to the yeast nucleus by nuclear localization sequences (NLS) that are an intrinsic part of the GAL4 DNA-BD. An additional gene of interest can be cloned into MCS II which is located downstream of an HA epitope and a second NLS. The resulting fusion protein is conditionally expressed from the Met25 promoter in response to methionine levels in the medium; i.e., it is repressed in the presence of 1 mM methionine and expressed in the absence of methionine.
酵母单杂交系统 Clontech pHis2说明书
pHIS2 is a reporter vector that can be used in yeast one-hybrid assays to identify and characterize DNA-binding proteins. The vector was specifically designed for use with the BD Matchmaker One-Hybrid Library Construction & Screening Kit (#K1617-1). It contains a HIS3 nutritional reporter gene, located downstream of a multiple cloning site (MCS) and the minimal promoter of the HIS3 locus (PminHIS3).Cis-acting DNA sequences, or DNA target elements, can be inserted into the MCS and used as baits to screen GAL4 AD/cDNA fusion libraries for proteins that interact with the target sequence. A protein-DNA (or one-hybrid) interaction can be detected by performing the assay in a yeast strain such as Y187 that is auxotrophic for histidine. Positive one-hybrid interactions drive expression of the HIS3 reporter gene, which enables the host cell to grow on histidine-deficient media.
In the absence of activation, the constitutive HIS3 expression from PminHIS3 is very low. During library screening, the leaky expression of HIS3 is controlled by adding 3-ami,2,4-triazole (3-AT) to the medium. The concentration of 3-AT needed to fully suppress leaky HIS3 expression must be determined empirically for each DNA target element.
pHIS2 can be maintained in both yeast and bacteria. It contains an autonomous replication sequence (ARS4) and TRP1 nutritional marker for replication and selection in yeast (1, 2); it contains a Col E1 origin and a kanamycin resistance gene (Kanr) for propagation and selection in E. coli. The centromeric sequence CEN6 ensures proper segregation of the plasmid during cell division in yeast (1, 2).
To use pHIS2 in a one-hybrid assay, clone one or more copies of a cis-acting DNA target sequence into the MCS. Then introduce the plasmid into competent yeast cells using the transformation protocol in the BD Matchmaker Library Construction & Screening Kits User Manual (PT3529-1). In contrast to the original BD Matchmaker One-Hybrid System, this reporter vector does not need to be integrated into the yeast genome. Instead, it is maintained as an episome throughout the assay. Inserting your target element may alter the level of background HIS3 expression. Therefore, constructs should be tested for background (leaky) HIS3 expression before you start a one-hybrid analysis. Background growth due to leaky HIS3 expression is controlled by adding 3-AT to the selection medium, as described in the User Manual (PT3529-1).
Multiple cloning sites: 141
HIS3 gene: 152811
Fragment containing the HIS3 3′ UTR & Termination sequence: 8121446
TRP1 gene: 28553529
Fragment containing the Col E1 E. coli origin of replication: 41654615
Kanamycin-resistance gene: 56054811
CEN6/ARS4 sequences: 62545737
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部分产品目录
Brand | Cat. # | Product | Package Size |
clontech | 636153 | Human Aorta Poly A+ RNA | 5 ug |
clontech | 636170 | Human Blood, Peripheral Leukocytes Poly A+ RNA | 5 ug |
clontech | 636113 | Human Heart Poly A+ RNA | 5 ug |
clontech | 636171 | Human Heart, Auricle Dextra (right) Poly A+ RNA | 5 ug |
clontech | 636172 | Human Heart, Auricle Sinistra (left) Poly A+ RNA | 5 ug |
clontech | 636175 | Human Heart, Pericardium Poly A+ RNA | 5 ug |
clontech | 636173 | Human Heart, Ventricle (left) Poly A+ RNA | 5 ug |
clontech | 636174 | Human Heart, Ventricle (right) Poly A+ RNA | 5 ug |
clontech | 636143 | Human Lymph Node Poly A+ RNA | 5 ug |
clontech | 636121 | Human Spleen Poly A+ RNA | 5 ug |
clontech | 639537 | SMARTScribe Reverse Transcriptase | 100 Rxns |
clontech | 634925 | SMARTer PCR cDNA Synthesis Kit | 10 Rxns |
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