DNA Vectors
GLPBIO TECHNOLOGY INC mCherry mRNA (5'CAP) 500ug
mCherry mRNA (5'CAP) is a commonly used fluorescent reporter gene in molecular biology research, with a Cap 1 cap structure and a poly(A) tail.
Agilent Technologies PSHUTTLE-CMV LACZ VECTOR
PShuttle-CMV lacZ Vector is a control vector produced by insertion of the lacZ gene in the multiple cloning site of the pShuttle-CMV. This construct is provided as a control for the production of recombinant adenovirus
New England Biolabs, Inc. Lambda DNA (dam-) – 250 µg
Duplex DNA is isolated from bacteriophage lambda (cI857ind 1 Sam 7). The bacteriophage is grown in an E. coli host which is deficient in adenine methylase (dam-). Therefore, those deoxyadenosine positions which are methylated in a wild type E. coli host are not methylated in the dam- host. This DNA gives complete digests with restriction endonucleases that are sensitive to dam methylation. Lambda DNA (dam-) is 48,502 base pairs in length.
New England Biolabs, Inc. PhiX174 RF I DNA – 30 µg
This is the double-stranded, covalently closed, circular form of X174 RF I DNA (supercoiled). The molecular weight of X174 RF I is 3.50 x 10^6 daltons and it is 5,386 base pairs in length. The vast majority of the molecules are RF I, and the remainder are RF II, as determined by agarose gel electrophoresis.
New England Biolabs, Inc. pBR322 Vector – 50 µg
pBR322 DNA is a commonly used plasmid cloning vector in E. coli and is a double-stranded circle 4,361* base pairs in length. pBR322 contains the genes for resistance to ampicillin and tetracycline, and can be amplified with chloramphenicol. The molecular weight is 2.83 x 10^6 daltons.
HORIZON DISCOVERY BIOSCIENCES LIMITED EDIT-R INDUCIBLE CAS9 LENTIVIR
Edit-R Inducible Lentiviral Hef1A-Blast-Cas9 Nuclease Particles (50 Ul, 10^7 Tu/Ml)
New England Biolabs, Inc. pBR322 Vector – 250 µg
pBR322 DNA is a commonly used plasmid cloning vector in E. coli and is a double-stranded circle 4,361* base pairs in length. pBR322 contains the genes for resistance to ampicillin and tetracycline, and can be amplified with chloramphenicol. The molecular weight is 2.83 x 10^6 daltons.
New England Biolabs, Inc. PhiX174 Virion DNA – 50 µg
ΦX174 Virion DNA is the single-stranded viral DNA isolated from bacteriophage ΦX174 am3 cs70. It has a molecular weight of 1.70 x 10^6 daltons and is 5386 bases in length. Greater than 85% of the molecules are circular.
New England Biolabs, Inc. pUC19 Vector – 250 µg
pUC19 is a commonly used cloning vector that conveys the Amp resistance. The molecule is a small double-stranded circle, 2686 base pairs in length, and has a high copy number. pUC19 carries a 54 base-pair multiple cloning site polylinker that contains unique sites for 13 different hexanucleotide-specific restriction endonucleases.
Agilent Technologies ADEASY ADENOVIRAL VECTOR SYSA
AdEasy Adenoviral Vector System employes Homologous recombination in E.coli. It has High-level protein expression. Infects both dividing and non-dividing cells with 100% transduction efficiency. Vitality hrGFP reporter is available.
Vector Biolabs GFP expressing RGD fiber modified Adenovirus (Ad(RGD)-CMV-GFP)
Ready to use in vivo grade AAV and Adenovirus Ready to use in vivo grade AAV and Adenovirus pre synthesized DNA vector High titer viral vectors 1/EA
MOLECULAR DEPOT LLC Enzyme Acceptor Buffer - 50 mL
Beta-galactosidase Enzyme Acceptor Stabilization Buffer (50 mL) consists of a buffer specifically optimized to stabilize the beta-galactosidase fragment known as enzyme acceptor (Omega fragment) The buffer can extend the shelf life of the enzyme acceptor to up to 12 months at 2-8C Without this buffer the enzyme acceptor is highly instable and loses activity at a high rate For in vitro research use only
New England Biolabs, Inc. PhiX174 RF I DNA – 150 µg
This is the double-stranded, covalently closed, circular form of X174 RF I DNA (supercoiled). The molecular weight of X174 RF I is 3.50 x 10^6 daltons and it is 5,386 base pairs in length. The vast majority of the molecules are RF I, and the remainder are RF II, as determined by agarose gel electrophoresis.
