Modifying Enzymes
Bioworld RNase A (Ribonuclease A), 250 mg
RNase A Source: Bovine pancreas Activity (Kunitz, Protein @37°)- >60U/mgProtease freeUnit definition: one Kunitz unit of RNase activity causes the decrease in absorbance from A0 to Af per minute at 25°C at 400nm (yeast RNA substrate).Applications: For use in DNA analysis or used to depolymerize viscous cell extract.
Bioworld Alkaline Phosphatase, 2500 Unit(s)
Alkaline Phosphatase1,000 UConjugation GradeAmmonium Sulfate SuspensionSource: Calf Intestine Adenosine Deaminase: <=0.001%Concentration (37 C): >7500U/mlPhosphodiesterase: <=0.001%DNase, RNase, and Protease: NoneSpecific activity (37 C, pH 10.5, DEA): >1500U/mg
Echelon Biosciences Research Labs cAMP Dependent Protein Kinase Inhibitor (PKI 5-24) - 1 mg, CAS#: 99534-03-9
cAMP Dependent Protein Kinase Inhibitor (PKI 5-24) - 1mg , Thr-Thr-Tyr-Ala-Asp-Phe-Ile-Ala-Ser-Gly-Arg-Thr-Gly-Arg-Arg-Asn-Ala-Ile-His-Asp-OH This item is non returnable
Echelon Biosciences Research Labs cAMP Dependent Protein Kinase Inhibitor 5-24 amide - 0.5 mg, CAS#: 100853-58-5
cAMP Dependent Protein Kinase Inhibitor 5-24 amide - 0.5mg , Thr-Thr-Tyr-Ala-Asp-Phe-Ile-Ala-Ser-Gly-Arg-Thr-Gly-Arg-Arg-Asn-Ala-Ile-His-Asp-NH2 This item is non returnable
Echelon Biosciences Research Labs cAMP Dependent Protein Kinase Inhibitor 5-24 amide - 1 mg, CAS#: 100853-58-5
cAMP Dependent Protein Kinase Inhibitor 5-24 amide - 1mg , Thr-Thr-Tyr-Ala-Asp-Phe-Ile-Ala-Ser-Gly-Arg-Thr-Gly-Arg-Arg-Asn-Ala-Ile-His-Asp-NH2 This item is non returnable
Creative Biomart Leukocyte Elastase Inhibitor (LEI)
Recombinant Leukocyte Elastase Inhibitor (LEI) Protein(His17-Glu332) is produced by E. coli expression system and fused with two N-terminal Tags, His-tag and T7-tag.
Enzo Life Sciences UbcH12 (human), (recombinant) (His-tag) (100 µg)
Purity: ≥95% (SDS-PAGE). Formulation: Liquid. In HEPES, pH 7.5, containing 100mM NaCl, 1mM DTT, 10% glycerol. Source: Produced in E. coli BL21 (λDE3). UbcH12 is fused to an N-terminal His-tag. Long Term Storage: -80°C.
Bioworld Trypsin, TPCK-Treated, 100 mg
Protease which cleaves specifically at the -COOH side of arginie and lysine. TPCK-treated Trypsin is a serine endopeptidate. Trypsin is treated with TPCK to inactivate any remaining chymotryptic activity. This type of trypsin is modified by acetyltion of the sigma-amino groups of lysine residues to prevent autolysis.
Cayman Chemical Oleoyl-D-lysInsodIum salt 25mg
An inhibitor of GlyT2a; selectively inhibits GlyT2a (IC50 = 48.3 nM) over GlyT1b (IC50 = >3,000 nM) in Xenopus oocytes expressing the human transporters; reduces allodynia in a nerve ligation rat model of neuropathic pain at 30 mg/kg, i.p.
Medchemexpress LLC Β-amylase, bacilus subtilis | 9000-91-3 | ≥50 U/mg solid | 1 G
Β-Amylase, Bacilus subtilis has abundant starch degrading activities and can be used for various biochemical studies. This product is for research use only and is not sold to patients.
- Has abundant starch degrading activities
- Suitable for various biochemical studies
- Appearance: Solid
- Color: White to off-white
- For research use only
ABclonal Technology Exonuclease I (E. coli)
Exonuclease I catalyzes the removal of nucleotides from single-stranded DNA in the 3 to 5 direction, and does not degrade DNA strands with the 3-OH end blocked by phosphoryl or acetyl groups. Exonuclease I has strict substrate specificity and is incapable of degrading double-stranded DNA and RNA.
ABclonal Technology Exonuclease VII
Exonuclease VII (Exo VII) can cleave single-stranded DNA in both 5-3 and 3-5 directions and is inactive against linear or circular double-stranded DNA. When PCR requires stepwise completion to obtain the final target product, this enzyme can be used to remove residual oligonucleotide primers left during intermediate stages of PCR, eliminating interference with subsequent use of different primers. The enzymes digestion of single-stranded DNA is independent of metal ions. This product is a highly purified protein obtained through the recombinant expression of the Exonuclease VII gene (XseA and XseB).
Medchemexpress LLC ADAMTS-5 Inhibitor 50mg | 929634-33-3 | 449.92 g·mol⁻¹ | C16H11ClF3N3OS3 | 50 MG
ADAMTS-5 Inhibitor is a small-molecule research compound that potently inhibits ADAMTS-5 (aggrecanase-2) with an IC50 of 1.1 μM and shows >40-fold functional selectivity over ADAMTS-4. It is supplied as a solid with a reported purity of 99.59%, a molecular weight of 449.92 g·mol⁻¹, and formula C16H11ClF3N3OS3. For research use only.
- Potent ADAMTS-5 inhibition (IC50 1.1 μM).
- Greater than 40-fold functional selectivity over ADAMTS-4.
- High reported purity of 99.59%.
- Supplied as a solid; also available as a 10 mM solution in DMSO.
- Available in multiple milligram packaging options (5 mg-500 mg) and larger quantities on request.
- Intended for research use only.