DNA Vectors
Vector Biolabs pre-synthesized DNA vector
Cyclin-dependent kinase 5 regulatory subunit 1 (p35) Adenovirus (Ad-p35)
BIOHIPPO Empty Vector CMV-Flag/BFP/BSD
Empty Vector CMV-Flag/BFP/BSD lentiviral vector expressing BFP under CMV promoter Each vial provides a nominal titer of 2x10E6 transducing units TU Lentiviral particles packaged with Empty Vector Ctrl ORF cDNA Lentivirus CMV promoter drives expression of fluorescent reporter and resistance marker separated by P2A An epitope tag remains upstream of the fluorescent reporter separated by T2A and would otherwise be C-terminal to the ORF cDNA which is not present in this empty vector control This product is great for use as a negative control for any of our ORF cDNA lentiviral particles You can choose the empty vector construct containing the epitope tag reporter and selection marker to match the ORF cDNA lentivirus product you are using The transduced cells will express all these components without any ORF cDNA insert Vector Layout 5 LTR-CMV-[no cDNA]-tag-T2A-Reporter-P2A-Selection-3 LTR
BPS Bioscience Inc ARE LUCIFERAS RPT LENT 2X500UL
The ARE Luciferase Reporter Lentivirus are replication incompetent, HIV-based, VSV-G pseudotyped lentiviral particles that are ready to be transduced into almost all types of mammalian cells, including primary and non-dividing cells. The particles contain a firefly luciferase gene driven by ARE located upstream of the minimal TATA promoter (Figure 1). After transduction, activation of the Nrf2 antioxidant response pathway in the target cells can be monitored by measuring the luciferase activity.Our products are for research use only, not for diagnostic or therapeutic use.BPS BIOSCIENCE INC mfg# 79869
IBA LifeSciences StrGate Acptr Vctr pASG-IBA103
The pASG-IBA103 vector is designed for expression of recombinant proteins with a C-terminal Twin-Strep-tag in E. coli. The vector carries an ampicillin resistance cassette for selection of transformed E. coli cells, F1 and ColE1 origin for a high plasmid copy number, and the inducible tetracycline promoter/operator for the regulated expression of proteins. The vector can be combined with any E. coli strain since the tet-promoter works independently of the genetic background of E. coli. Expression of the recombinant protein is induced by addition of anhydrotetracycline, which is a derivative of tetracycline that does not exhibit antibiotic activity. Please note that cloning into pASG-IBA Acceptor Vectors compulsorily requires the restriction enzyme Esp3I since no other MCS for the integration of a gene of interest is available. In addition to the direct cloning of the gene of interest into pASG-IBA vectors with Esp3I, another option via a so-called Entry Vector is possible.
IBA LifeSciences StrGat Acptr Vctr pENTRY-IBA51
StarGate Entry Vector is designed to insert the PCR product of a certain gene of interest (GOI) to generate a Donor Vector. StarGate cloning via the pENTRY-IBA vector provides a tool for the systematic and rapid screen of the best working expression conditions for a certain GOI, where nothing is known from literature. After initial pENTRY cloning, the GOI in the resulting Donor Vector can be easily transferred by a simple one-tube reaction into a multitude of expression vectors (Acceptor Vectors) providing different features.
IBA LifeSciences StrGate Acptr Vctr pASG-IBA45
The pASG-IBA45 vector is designed for expression of recombinant proteins with an N-terminal Strep-tagII and a C-terminal His-tag in E. coli. The vector carries an ampicillin resistance cassette for selection of transformed E. coli cells, F1 and ColE1 origin for a high plasmid copy number, the inducible tetracycline promoter/operator for the regulated expression of proteins. Expression of the recombinant protein is induced by addition of anhydrotetracycline, which is a derivative of tetracycline that does not exhibit antibiotic activity. Please note that cloning into pASG-IBA Acceptor Vectors compulsorily requires the restriction enzyme Esp3I since no other MCS for the integration of a gene of interest is available. In addition to the direct cloning of the gene of interest into pASG-IBA vectors with Esp3I, another option via a so-called Entry Vector is possible.
LTR228 Cell Line (ATCC HB-8502) - Human B-cell, derivative of WIL-2NS
LTR228 is a human B-cell lymphoid cell line reported as a derivative of the WIL-2NS parent line. It is used in immunology research and as a fusion partner for hybridoma production. The cell line is associated with ATCC catalog HB-8502.
- Human B-cell origin.
- Derived from WIL-2NS parent line.
- Reported tissue of origin: spleen.
- Common application: fusion partner for human B lymphocytes and immunology research.
- Synonyms include LTR 228 and LTR 228-TG.
Amsbio LLC SV40 Large T-antigen (CMV/ no selection) lentivirus
SV40 Large T-antigen (CMV no selection) lentivirus
IBA LifeSciences StrGate Acptr Vctr pASG-IBA4
The pASG-IBA4 vector is designed for expression of recombinant proteins with an N-terminal Strep-tagII in E. coli. The vector carries an ampicillin resistance cassette for selection of transformed E. coli cells, F1 and ColE1 origin for a high plasmid copy number, the inducible tetracycline promoter/operator for the regulated expression of proteins, and the ompA signal for periplasmic secretion of the recombinant protein. Expression of the protein is induced by addition of anhydrotetracycline, which is a derivative of tetracycline that does not exhibit antibiotic activity. During the secretion into the periplasmic space the ompA signal sequence will be cleaved off. Please note that cloning into pASG-IBA Acceptor Vectors compulsorily requires the restriction enzyme Esp3I since no other MCS for the integration of a gene of interest is available. In addition to the direct cloning of the gene of interest into pASG-IBA vectors with Esp3I, another option via Entry Vector is possible.