Modifying Enzymes
Cayman Chemical Decnoyl-Coenzyme Ahydrate 5mg
A thioester of decanoic acid and CoA; inhibits the activity of mitochondrial CS and GDH isolated from rat brain (IC50s = 437 and 420 µM, respectively); inhibits FadR from binding its promoter in E. coli (Ki = 2 µM); produced during isomerase-dependent β-oxidation of oleic acid in isolated rat heart mitochondria
Bio IVT CYP2C8 Low Reductase Bactosomes, Human rCYP Enzyme, 1 nmol/vial.
CYP2C8 Low Reductase Bactosomes, Human rCYP Enzyme, 1 nmol/vial.
Medchemexpress LLC Hyaluronidase, ovine testes | 37326-33-3 | MFCD00131351 | 95.0% | 55,000 g/mol | 5 MG
Hyaluronidase, ovine testes is a protein enzyme preparation that hydrolyzes hyaluronic acid in extracellular matrices. Supplied as a lyophilized powder, it is intended for use in biochemical assays, tissue dissociation, and reproductive biology research where controlled degradation of hyaluronic acid is required.
- Enzymatic degradation of hyaluronic acid for tissue dissociation and analytic assays.
- Derived from ovine testes for endogenous enzyme activity profile.
- High purity to minimize contaminating proteins and activities (95.0%).
- Average molecular weight approximately 55,000 g/mol for preparative considerations.
- Supplied in small pack sizes suitable for research-scale experiments.
Discovery Life Sciences HUMAN FM05
Human FMO5 SUPERSOMES 2.5 mg protein in 0.5mL This activity is catalyzed by FMO5 which is expressed from human FMO5 cDNA using a baculovirus expression system
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 TAOK2/10UG/CATALYTIC
TAOK2, Catalytic domain, Wild type, Amino Acid 1-319, NP_004774.1, Expressed in Insect (sf21); 10microg
Qiagen Beverly Inc KLENOW FRAGMENT
DNA Polymerase; Klenow Fragment; Conc. 5,000 U/ml; 2,500 U; incl. 10X buffer
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
ABclonal Technology Endonuclease VIII
Endonuclease VIII originates from E.coli and possesses both N-glycosylase and AP-endonuclease activity. The N-glycosylase activity releases damaged pyrimidines from double-stranded DNA, generating an apurinic (AP site). The AP-endonuclease the phosphodiester bond at the AP site, forming 3’-P and 5’-P ends. Damaged bases recognized and removed by Endonuclease VIII include: urea, 5, 6-dihydroxythymine, thymine glycol, 5-hydroxy-5-methylhyd antoin, uracil glycol, 6-hydroxy-5, 6-dihydrothymine and methylhydroxy- methyluracil.
Cusabio Technology LLC Acetyl-CoA carboxylase 1
This kit detects ACACA (Acetyl-CoA carboxylase 1) in human serum plasma tissue homogenates and cell lysates using a sandwich ELISA methodology It offers a quantitative detection range of 9 38 pg/mL to 600 pg/mL with a sensitivity of 2 34 pg/mL ensuring precise measurement of low-abundance samples The assay requires a short incubation period of 1-5 hours and utilizes a sample volume of 50-100 L per test Results are determined by absorbance measurement at 450 nm providing a reliable and standardized approach for ACACA analysis in research or diagnostic applications The kit s optimized protocol maintains specificity and reproducibility across diverse biological matrices making it suitable for studies involving lipid metabolism regulation enzyme activity monitoring or biomarker discovery related to ACACA expression
ABclonal Technology Exonuclease III (E. coli)
Exonuclease III (E.coli) catalyzes the stepwise removal of mononucleotides from 3?-hydroxyl termini of duplex DNA. The preferred substrates are dsDNA with blunt or recessed 3?-, termini although the enzyme also acts at nicks in dsDNA to produce single-strand gaps. dsDNA with 3?-overhang are resistant to cleavage; when overhangs length is ≥ 4 bases，dsDNA are able to fully prevent ExoIII cleavage process. Exonuclease III has also been reported to have RNase H, 3?-phosphatase and AP-endonuclease activities.