Modifying Enzymes
Sigma Aldrich Fine Chemicals Biosciences Proteinase K from Tritirachium album Reagents designed and manufactured under current ISO 13485 certification. | 39450-01-6 | MFCD00132129 | 5ML
Proteinase K from Tritirachium album Reagents designed and manufactured under current ISO 13485 certification. | 39450-01-6 | MFCD00132129 | 5ML
Cayman Chemical Oleoyl-L-carnItIn 10mg
A long-chain acylcarnitine and GlyT2 inhibitor (IC50 = 340 nM); selective for GlyT2 over GlyT1 (IC50 = >10,000 nM); plasma levels are increased in patients with chronic kidney disease or end-stage renal disease receiving incident hemodialysis and these are associated with cardiovascular mortality
![Medchemexpress LLC N-cyclobutyl-6-[2-(3-fluorophenyl)ethynyl]-3-pyridinecarboxamide | 1310012-12-4 | 98.1% | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000234369.png-250.jpg)
Medchemexpress LLC N-cyclobutyl-6-[2-(3-fluorophenyl)ethynyl]-3-pyridinecarboxamide | 1310012-12-4 | 98.1% | 50 MG
VU0360172 is a potent and selective positive allosteric modulator of the metabotropic glutamate receptor 5 (mGlu5) used as a research reagent for cellular and in vivo pharmacology studies.
- Potent mGlu5 positive allosteric modulation (EC50 16 nM).
- Binding affinity to mGlu5 (Ki 195 nM).
- High purity suitable for research (98.1%).
- Molecular formula C18H15FN2O and molecular weight 294.32 g/mol.
- Solid, light yellow to brown research material supplied as 50 MG quantities.
Cayman Chemical N-Oleoyl ProlIn 1mg
An endogenous N-acyl amine that is decreased in lumbar spinal cord after capsaicin administration (1 UG/10 µl) and has surfactant properties (critical micelle concentration = 4.8 µM)
Cayman Chemical Monoacylglycerol Lipase FL P
Immunogen: Purified recombinant human MAGL • Host: Rabbit • Species Reactivity: (+) Human and rat; other species not tested • Applications: ICC, IHC, and WB
Apexbio Technology LLC EZ Cap CM-EGFP Probe mRNA (m1Ψ) 5x1mg (1mg/mL)
CM-EGFP mRNA encodes a fusion protein comprised of a cell membrane (CM) targeting signal sequence and enhanced green fluorescent protein (EGFP) By fusing EGFP with a membrane localization signal this probe enables real-time visualization of dynamic changes occurring at the cell membrane of living cells particularly beneficial for research involving cell membrane-related processes such as signal transduction membrane protein interactions and alterations in membrane structure EZ Cap CM-EGFP Probe mRNA (m1 ) is provided at 1 mg/mL It is specifically designed for cell membrane-specific expression of a green fluorescent protein label This mRNA is synthesized through co-transcriptional capping resulting in a Cap 1 structure The incorporation of m1 modifications poly(A) tail significantly enhances mRNA stability and lifetime both in vitro and in vivo
Carnabio Usa Inc QIK(SNF1LK2)/10UG/FULL-LENGTH
QIK(SNF1LK2), Full-length, Wild type, Amino Acid 1-926, NP_056006.1, Expressed in Insect (sf21); 10microg
New England Biolabs, Inc. Endonuclease VIII – 5000 units
Endonuclease VIII from E. coli acts as both an N-glycosylase and an AP-lyase. The N-glycosylase activity releases damaged pyrimidines from double-stranded DNA, generating an apurinic (AP site). The AP-lyase activity cleaves 3' and 5' to the AP site leaving a 5' phosphate and a 3' phosphate. Damaged bases recognized and removed by Endonuclease VIII include urea, 5, 6- dihydroxythymine, thymine glycol, 5-hydroxy-5- methylhydantoin, uracil glycol, 6-hydroxy-5, 6-dihydrothymine and methyltartronylurea. While Endonuclease VIII is similar to Endonuclease III, Endonuclease VIII has and lyase activity while Endonuclease III has only lyase activity.
Medchemexpress LLC Amylase | 9000-92-4 | 5 G
Amylase is an enzyme produced by the pancreas and salivary glands, catalyzing the hydrolysis of starch into sugars. Amylase is broadly classified into α, β, and γ subtypes.
- It is an enzyme produced by pancreas and salivary glands.
- It catalyzes the hydrolysis of starch into sugars.
- Amylase is classified into α, β, and γ subtypes.
ABclonal Technology T4 DNA Ligase (High Conc.)
T4 DNA Ligase catalyzes the formation of a phosphodiester bond between juxtaposed 5 phosphate and 3 hydroxyl termini in duplex DNA or RNA. This enzyme will join blunt end and cohesive end termini as well as repair single stranded nicks in duplex DNA and some DNA/RNA hybrids. T4 DNA ligase will seal nicks for these DNA substrates. T4 DNA Ligase is applicable to cloning of restriction fragments and to joining linkers and adapters to blunt-ended DNA.
![Amsbio LLC Neuraminidase isozyme S [Reagent for studies of gangliosides]](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502566244.png-250.jpg)
Amsbio LLC Neuraminidase isozyme S [Reagent for studies of gangliosides]
Neuraminidase isozyme S [Reagent for studies of gangliosides]
Athens Research And Technology Inc PLASMINOGEN HU 1MG
Plasminogen, Human Plasma: 1 MG; Lyophilized from 20 mM Tris-HCl, pH 7.5, with 2 mM EDTA; MW 90,000-92,000; EC=1.71; Activity: > 120 units/mg protein; Purity: > =95% by SDS-PAGE. Native; Purified from human plasma in the Athens Research & Tech lab.
Sigma Aldrich Fine Chemicals Biosciences beta-N-Acetylglucosaminidase from Streptococcus pneumoniae recombinant, expressed in E. coli, buffered aqueous solution | 9012-33-3 | MFCD00081402 | 1VL
beta-N-Acetylglucosaminidase from Streptococcus pneumoniae recombinant, expressed in E. coli, buffered aqueous solution | 9012-33-3 | MFCD00081402 | 1VL
INTACT GENOMICS INC Cas12a Nuclease 400 µg
Intact Genomics (ig) Cas12a Nuclease is the purified recombinant Francisella tularensis Cas12a enzyme for in vitro editing. This enzyme is designed to perform CRISPR/Cas12a-mediated genome editing. The physical purity of this enzyme is ≥65% as assessed by SDS-PAGE with Coomassie blue staining and densitometry.Product Components: Cas12a Nuclease 10x Cas12a Nuclease Reaction Buffer