SimpleSeq DNA sequencing kits provide a simple, fast, and convenient way to order and use DNA sequencing reactions

Hooke Kits™ for EAE Induction in C57BL/6 Mice. Emulsion supplied in pre-filled syringes, ready to use. Consistently induces EAE in female C57BL/6 mice EAE will develop in 90-100% of mice. Disease onset is 9 to 14 days after immunization. Mean maximum score will be 3.0 to 3.5. Each lot is tested and individually adjusted to ensure consistent disease induction. On Day 0, MOG35-55/CFA or MOG1-125/CFA emulsion and pertussis toxin are injected. On Day 1, a second dose of pertussis toxin is injected.roperly prepared emulsions are critical for reliable induction of many autoimmune disease models. Our emulsions are carefully made and pre-filled into syringes, ready to use, to reduce time needed to set up experiments.Lot-to-lot reagent variations can cause dramatic changes in severity of induced autoimmune disease.

The QuickTiter MuLV Core Antigen ELISA Kit measures the core antigen of MuLV with sensitivity as low as 300 pg/mL. Reagents are sufficient for 96 wells including standards and unknown samples.

MCSG1 CRYSTALLIZATION SCREEN (1.7 ML DEEP WELL BLOCK).

EZ-Tn5™ Transposase is a hyperactive Tn5 transposase for random insertion of an EZ-Tn5 Transposon into any cloned DNA in vitro or for preparing an EZ-Tn5 Transposome for random insertion of a EZ-Tn5 Transposon into the genomic DNA of living bacteria.

Trypsin-EDTA for Primary Cells is a low-concentration formulation (0.05% Trypsin and 0.02% EDTA in phosphate buffered saline without calcium or magnesium) of porcine pancreatic trypsin and EDTA that is suitable for the dissociation of cell monolayers that are susceptible to "over-trypsinization." These adherent cells include primary cells (i.e., ATCC Primary Cells Solutions™ cell types) as well as a variety of mammalian cell lines that are propagated in serum-free or low serum conditions. For use by FOR-PROFIT companies only; NON-PROFIT companies use 50189662NP. New ATCC customers are required to register with ATCC prior to purchase. The application can be found at https://www.atcc.org/en/My_Profile/Register.aspx

Trypsin Neutralizing Solution is specifically formulated (5% FBS in phosphate buffered saline without calcium and magnesium) to rapidly inactivate the concentration of trypsin found in the Trypsin-EDTA for Primary Cells solution. For use by FOR-PROFIT companies only; NON-PROFIT companies use 50189663NP. New ATCC customers are required to register with ATCC prior to purchase. The application can be found at https://www.atcc.org/en/My_Profile/Register.aspx

RapidStart NADPH Regenerating System, 5 vial kit

SignalFire ECL Reagent 500 ml

Pooled Cynomolgus monkey liver cytosol, male, 1.0 ML at 10 ME/ML (10 ME)

Glyko� 2-AB Bovine Fetuin N-linked Glycan Library [GKSB-002]

RapidStart NADPH Regenerating System

Tacha's Automated Hematoxylin is a water-based hematoxylin, specially formulated for automated IHC. This hematoxylin can be used on FFPE or frozen tissue. Nuclei stain a sky blue, providing high contrast staining.

Rho/Rac/Cdc42 Activator I

5 mL of mineral oil solution (Incomplete Freund's Adjuvant)

Forskolin 10 mg

Bisindolylmaleimide I, Hydrochloride 500 µg

H-89, Dihydrochloride 5.19 mg

Anti-mouse IgG (H+L), F(ab')2 Fragment (Alexa Fluor 647 Conjugate) 250 µl

DAB Sparkle is a specially formulated ready-to-use enhancing solution that will increase sensitivity and contrast of DAB stained tissues.

The Rat-on-Mouse HRP-Polymer is for use with rat primary antibodies on mouse tissues. This detection system is mouse adsorbed for minimum cross-reactivity to endogenous mouse IgG. It is labeled with horseradish peroxidase (HRP).

CRISPRtest™ Functional Cas9 Activity Kit for Human Cells

The kit randomly inserts a KanR gene and a R6Ky origin of replication into any cloned DNA for rescuing plasmids not normally replicated in E. coli.

Normal sera are used to counteract the non-specific interaction between the sample and immunoglobulins. They can be added to the blocking solution and the incubation media. As a rule the normal serum species should be the same as the secondary antibody species (use normal goat serum with goat-anti-rabbit conjugates). Note: normal sera should not be used in combination with Protein A and Protein G gold reagents.