DNA Vectors
Sino Biological pCMV3-N-GFPSpark Control Vector (N-terminal GFPSpark-tagged) 1Unit
N-terminal GFPSpark-tagged pCMV3 Control Vector
System Biosciences LLC Cre Recombinase Expression Plasmid (pCMV-CRE) | 10ug
With the Cre-LoxP site-specific recombination system used in most of our HR Targeting Vectors, you can get rid of extra sequences, such as selection cassettes, by transiently expressing the Cre recombinase from the pCMV-CRE Cre Recombinase Expression Plasmid.
LifeSensors PE-SUMOSTAR KAN 20UG
The pE-SUMOstar vector is for the expression of recombinant SUMOstar fusion proteins (containing an N-terminal His6 tag) in E. coli. Production is driven by T7 RNA polymerase-promoter system, with kanamycin resistance facilitating plasmid selection and stability.
Agilent Technologies PSHUTTLE VECTOR
pShuttle Vector is a containing only a multiple cloning site in which an entire expression cassette can be inserted.THis vector contains the kanamycin resistance gene for the selection of recombinants
Expression Systems PVL1393 TRANSFER VECTOR
pVL1392 and pVL1393 are transfer vectors designed for high-level expression of a cloned gene driven by the strong Autographa californica multiple nucleopolyhedrovirus (AcMNPV) polyhedrin promoter (pPolh).
pVL1392 and pVL1393 are pUC8 based plasmids containing the AcMNPV polyhedrin locus lacking the majority of the polyhedrin open reading frame. A multiple cloning site (MCS) sequence has been inserted 37 nucleotides downstream from the original polyhedrin ATG start codon, which has been mutated to ATT.
pVL1392 and pVL1393 share identical sequences, with the exception that they each have the same MCS in opposing orientations. A start and stop codon must be provided with the gene that is to be cloned into the MCS. For maximal recombinant protein expression, the distance between the cloning site and the ATG start of the inserted gene should be kept to a minimum, and should not exceed 100 nucleotides.
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.
Abcam pCambia0380 Plant Expression Vector
pCambia0380 Plant Expression Vector
The product is subject to the following: Abcam Restricted Use Statement
Abcam pCambia1300 Plant Expression Vector
pCambia1300 Plant Expression Vector
The product is subject to the following: Abcam Restricted Use Statement
Abcam pCambia1301 Plant Expression Vector
pCambia1301 Plant Expression Vector
The product is subject to the following: Abcam Restricted Use Statement
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. 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.
Creative Biomart Recombinant Streptococcus pneumoniae type 19a Capsular Polysaccharide Diphtheria CRM197 Protein Conjugate Antigen
Streptococcus pneumoniae type 19a capsular polysaccharide diphtheria crm197 protein conjugate antigen is a sterile vaccine that contains saccharides of the capsular antigens of Streptococcus pneumonia