E.coli UDG
Syd Labs E.coli UDG UDG MB124, cheapest heat-labile UDG (Uracil DNA Glycosylases, UNG) and E.coli UDG for LAMP, PCR/qPCR, and RT-PCR/RT-qPCR. Low price of bulk heat-labile UDG and E.coli UDG. Order now!
Syd Labs E.coli UDG UDG MB124, cheapest heat-labile UDG (Uracil DNA Glycosylases, UNG) and E.coli UDG for LAMP, PCR/qPCR, and RT-PCR/RT-qPCR. Low price of bulk heat-labile UDG and E.coli UDG. Order now!
Syd Labs Heat-Labile UDG MB123, cheapest heat-labile UDG (Uracil DNA Glycosylases, UNG) and E.coli UDG for LAMP, PCR/qPCR, and RT-PCR/RT-qPCR. Low price of bulk heat-labile UDG and E.coli UDG. Order now!
Syd Labs PCR Enhancer MB040-EE-1, Cheap GC rich PCR enhancer to improve efficiency of PCR amplification of GC rich DNA templates, increase specificity of PCR products, and reduce non-specific and undesirable PCR products. Promotion: Buy...
Syd Labs Spin Column for DNA/RNA Tiniprep MB0110, The spin columns for small volume DNA elution, small amount DNA extraction and DNA concentration, small volume RNA elution, small amount RNA extraction and RNA concentration are...
Extensive experience with making DNA constructs for Fc fusion protein production, expressing and purifying a number of Fc fusion proteins from microgram to kilogram scales in mammalian cells, such as CHO and HEK 293 cells.
We provide the services of developing stable cell lines for: G-Protein Coupled Receptors (GPCR) of high pharmacological relevance; other cell-based assays such as ion channel and kinases (RTKs).
Fast stable cell line generation service for antibody production: development of suspension CHO stable cell lines for antibody production. No virus involved. DNA Transfection and stable cell line screening only.
Fast stable cell line development services for protein expression: development of suspension CHO stable cell lines expressing recombinant proteins. No virus involved. DNA Transfection and stable cell line screening only.
Engineer or genetically modify bacterial strains, such as E. coli and Lactococcus lactis, to achieve protein overproducttion or gene silencing, stable labelling for tracing cell specificiation.
Knock-out and knock-in cell lines are generated using the powerful CRISPR/Cas9 genome editing tool. Knock-out and knock-in cell line development with any gene and any host cell, including mammalian primary cell, without introducing foreign DNA.