Please ensure Javascript is enabled for purposes of website accessibility
Contact us Contact Us
EN
Home > Products > Recombinant Proteins > Enzyme

Enzymes & Kinases

Explore bioactive recombinant enzymes and kinases for signaling, proteolysis, and post-translational modification studies. Expressed in HEK293, CHO, or E. coli, each lot is activity-verified with specific units (U/mg or mU/µg) and documented assay conditions (substrate, pH, cofactors). Options include carrier-free, His-tag, and Fc-fusion formats with low endotoxin for sensitive cell-based workflows. RUO

Why Researchers Choose abinScience

Activity-Verified With unit definition, acceptance criteria & method
High Purity Low endotoxin with lot-specific CoA
Multiple Hosts HEK293/CHO/E. coli for native PTMs or fast screening
Flexible Formats Carrier-free & tag options (His/Fc); lyophilized or liquid
Scalable & Global Sizes; cold-chain shipping

Popular Subcategories

Selection Guide

  1. Activity Readout: Confirm unit definition (U/mg), substrate & assay buffer; match to your platform (fluorescent/colorimetric/radio).
  2. Cofactors & Conditions: ATP/Mg2+/Mn2+, pH & temperature optima; check inhibitors/activators listed in the CoA.
  3. Expression System: HEK293/CHO for glycosylated enzymes and stability; E. coli for rapid screens.
  4. Endotoxin & Format: Choose low endotoxin and carrier-free for cell assays; select His/Fc tags per capture/purification needs.
  5. Specific Variants: WT vs. catalytic-dead/mutants for negative controls or mechanistic studies.

Applications

Signal transduction & phosphorylation cascades (kinase panels)
Dephosphorylation & pathway interrogation (PTPs/serine-threonine phosphatases)
Protease cleavage mapping, apoptosis & ECM remodeling (caspases/MMPs)
Ubiquitination/SUMOylation cycles, DUB screening
Glyco-engineering & receptor biology

Documents & QC

CoA with specific activity, method, substrate & conditions
SDS-PAGE/HPLC images; storage, stability & reconstitution

FAQs

How are enzyme “units” defined on your CoA?

Units reflect product formation or substrate turnover per time under stated conditions (substrate, buffer, pH, temperature, cofactors). Always replicate those conditions when comparing activity.

Which expression system should I choose?

Use HEK293/CHO for enzymes requiring glycosylation or complex folding; E. coli suits fast screens or tags not affecting function.

What endotoxin level is recommended for cell assays?

Typically ≤0.1 EU/µg. Verify the lot-specific CoA and include appropriate controls.

RUO disclaimer

All products are for Research Use Only and not for diagnostic procedures.

Options+
Options
Confirm
  • Product types
    0 selected
    Proteins (21)
  • Expression system
    0 selected
    E. coli (17)
    Mammalian Cells (2)
    Yeast (1)
  • Target
    0 selected
    M-MLV (1)
    Benzonase Nuclease/Endonuclease (1)
    α-fucosidase/AlfC (1)
    Lambda Protein Phosphatase (Lambda PP) (1)
    SUMO protease/ULP1 (1)
    IdeS Protease (IgG Specific) (1)
    CU43 Protease (Human IgG Specific) (2)
    Endo S (1)
    Endo S2 (1)
    CAT (1)
    T5 Exonuclease (1)
    IdeZ Protease (IgG Specific) (1)
    3C Protease (1)
    TEV Protease (1)
    Enterokinase (1)
    PNGase F (1)
    polA/Taq polymerase 1 (1)
  • Species
    0 selected
    Escherichia phage lambda (Bacteriophage lambda) (1)
    Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (1)
    Streptococcus pyogenes (3)
    Corynebacterium ulcerans (2)
    Human (1)
    Escherichia phage T5 (Enterobacteria phage T5) (1)
    Streptococcus equi (1)
    HRV-14 (1)
    Tobacco etch virus (TEV) (1)
    Homo sapiens (Human) (1)
    Bovine (2)
    Elizabethkingia miricola (1)
    Thermus aquaticus (1)
    MoMLV (1)
    Clostridium perfringens (1)
    Serratia marcescens (1)
    Lacticaseibacillus paracasei (Lactobacillus paracasei) (1)
  • Applications
    0 selected
    Recombinant Glycoprotein Expression (1)
    cDNA Synthesis (1)
    Beta-Hexosaminidase B can release all types of GlcNAc(β1-x) units (1)
    Glycoprotein Analysis (1)
    Endo S2 hydrolyses N-linked glycans on IgG and α1-acid glycoprotein. (1)
    Fusion Protein Cleavage (1)
    Colony PCR (1)
    Reverse Transcription (cDNA Synthesis) (1)
    including the bisecting GlcNAc structure in N-linked glycans. (1)
    Remove fusion tags from proteins with the HRV 3C cleavage sequence(LEVLFQ↓GP). (1)
    Protein Purification (1)
    TEV Protease is a highly specific cysteine protease. The TEV Protease recognition sequence with the highest catalytic efficiency is ENLYFQ↓(S/G/A/M/C/H). (1)
    Multiplex PCR (1)
    RT-PCR & cDNA Synthesis (1)
    Terminal transferase catalyzes the addition of deoxynucleotides to the 3' hydroxyl terminus of DNA molecules. (1)
    Protein Digestion (1)
    Specialty PCR (1)
    RT-qPCR (1)
    Removal of high mannose N-glycans from glycoproteins (1)
    Routine PCR (1)
    α-fucosidase/AlfC is a highly specific exoglycosidase that catalyzes the hydrolysis of alpha-1 (1)
    RT-PCR and cDNA Synthesis (1)
    Remove phosphate groups from phosphorylated serine (1)
    Neuraminidase (Sialidase) has been used to desialylate transferrin in order to study its isoforms in human serum. (1)
    Expression Systems (1)
    6-linked fucose residues from glycoproteins. (1)
    PCR (2)
    threonine and tyrosine residues in proteins. (1)
    Proteomics (6)
    Remove or cleave SUMO tag from the SUMO fusion protein (1)
    Glycan Sequencing (1)

Quick access

Contact Us

  • +86-027-65523339

  • info@abinscience.com

  • Building C, No. 666, Shen Dun Si Lu, Wuhan, 430206, China

Copyright © 2025 abinScience. All Rights Reserved. All Products are for Research Use Only