Comparative analysis of high-density polyethylene and polystyrene microplastics pollution: Uptake, elimination and results in mussel
The high-density polyethylene (HDPE) and the polystyrene (PS), that are typical microplastic contaminants, are ceaselessly detected within the surroundings and have potential hazard to environmental well being. On this research, the buildup, elimination, tissue distribution and potential results of the HDPE and the PS within the mussels (Mytilus galloprovincialis) have been evaluated. The HDPE and the PS have been present in varied tissues (digestive gland > gill > gonad ≈ muscle) with no distinction in distribution patterns. The buildup of the HDPE and the PS quickly elevated within the first 48 h publicity, and the buildup of HDPE was increased than that of PS. After 144 h of elimination, a lot of the HDPE and the PS have been cleared by mussels.
As well as, the actions of superoxide dismutase (SOD), catalase (CAT) and the content material of oxidized glutathione significantly elevated, indicating that the HDPE and the PS induced oxidative stress and prevented oxidative injury in elimination. The metabolomic evaluation prompt that publicity to HDPE and PS induced alterations within the metabolic profiles of mussel. Differential metabolites have been concerned in power metabolism, lipid metabolism, tricarboxylic acid cycle and neurotoxic response., and In the meantime, the PS had a decrease impact on mussel metabolism throughout elimination, however the impact of HDPE was elevated. General, this research elucidated that the HDPE and the PS brought about opposed results on the mussels and supplied insights towards understanding the hazard of various microplastics on aquatic organisms.
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Description: TNFR2 Human produced in E.Coli is a single, non-glycosylated polypeptide chain containing 184 amino acids and having a molecular mass of 20kDa. The TNFR2 is purified by proprietary chromatographic techniques.
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
Known also as Polyethylene Glycol elisa. Alternative names of the recognized antigen: PEO
POE
Polyethylene oxide
Polyoxyethylene
Carbowax
GoLYTELY
GlycoLax
Fortrans
TriLyte
Colyte
Halflytely
Macrogol
MiraLAX
MoviPrep
Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of General Polyethylene Glycol (PEG) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids with no significant corss-reactivity with analogues from other species.
Description: Torin2 is a potent, selective and orally available inhibitor of mTOR with EC50 value of 0.25nM [1].Torin2 is a highly potent and selective mTOR inhibitor.
Description: MI-2 is a Menin-MLL inhibitor with IC50 value of 0.45 ?M [1]. Mixed-lineage leukemia (MLL) is a common target of chromosomal translocations in patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL).
A monoclonal antibody specific to Polyethylene Glycol (PEG) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Polyethylene Glycol (PEG) and unlabeled Polyethylene Glycol (PEG) (Standards or sa
Description: A competitive Inhibition ELISA kit for detection of Polyethylene Glycol from General in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
High Sensitivity Polyethylene Glycol (PEG) ELISA Kit
Description: BNP Recombinant Human fused with 20 amino acid His tag at N-terminus produced in E.Coli is a single, non-glycosylated, polypeptide chain containing 129 amino acids (27-134 a.a) and having a molecular mass of 14 kDa.
Description: Interleukin-2 Human Recombinant produced in E.Coli is a single, non-glycosylated, Polypeptide chain containing 133 amino acids fragment (21-153) having a molecular weight of 20kDa and fused with a 4.5kDa amino-terminal hexahistidine tag. _x000D_ The IL-2 His is purified by proprietary chromatographic techniques._x000D_
BMP-2 Bone Morphogenetic Protein-2 Human Recombinant Protein, Monomer
Description: Bone Morphogenetic Protein-2 Human Recombinant produced in E.Coli is a monomeric, non-glycosylated, Polypeptide chain containing 115 amino acids (283-396) and having a molecular mass of 13009 Dalton. ;The BMP-2 is purified by proprietary chromatographic techniques.
Malaria P. falciparum Culture Panel FCQ79 (Type A) (16 X 200 µL)
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Buffer: Supplied at 1.0mg/mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Antibodies were produced by immunizing rabbits with synthetic peptide and KLH conjugates. Antibo
Description: A polyclonal antibody against MYOD1 (Ab-200). Recognizes MYOD1 (Ab-200) from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB;WB:1:500-1:1000
Buffer: Supplied at 1.0mg/mL in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Antibodies were produced by immunizing rabbits with synthetic peptide and KLH conjugates. Antibo
Description: A polyclonal antibody against MYOD1 (Ab-200). Recognizes MYOD1 (Ab-200) from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB;WB:1:500-1:1000
Description: A high purity chemical with various applications in medical research, drug-release, nanotechnology and new materials research, cell culture. In the study of ligand, polypeptide synthesis support, a graft polymer compounds, new materials, and polyethylene glycol-modified functional coatings and other aspects of the active compound.
Description: Can be used for various proteomics studies in both normal and pathological cases. It is an excellent control and suitable for educational purposes. This product is prepared from whole tissue homogenates and has undergone SDS-PAGE quality control analysis. The protein is stored in a buffer with protease inhibitor cocktail fo prevent degradation.
Description: Defensins (alpha and beta) are cationic peptides with a broad spectrum of antimicrobial activity that comprise an important arm of the innate immune system. The α-defensins are distinguished from the β-defensins by the pairing of their three disulfide bonds. To date, six human β-defensins have been identified; BD-1, BD-2, BD-3, BD-4, BD-5 and BD-6. β-defensins are expressed on some leukocytes and at epithelial surfaces. In addition to their direct antimicrobial activities, they can act as chemoattractants towards immature dendritic cells and memory T cells. The β-defensin proteins are expressed as the C-terminal portion of precursors and are released by proteolytic cleavage of a signal sequence and in some cases, a propeptide sequence. β-defensins contain a six-cysteine motif that forms three intra-molecular disulfide bonds. Recombinant human BD-2 is a 4.3 kDa protein containing 41 amino acid residues.
Description: Relaxin-2 is a peptide hormone structurally related to insulin, which is expressed in the placenta, decidua, prostate, and in the ovary during pregnancy. Of the three known relaxin genes, Relaxin-2 is the only relaxin known to circulate in the blood. Relaxin-2 binds specifically to the LGR7 and LGR8 receptors, previously identified as an “orphan” G protein coupled receptors. Signaling by Relaxin-2 through its target receptors enhances the growth of pubic ligaments and ripening of the cervix during birth. Recombinant Relaxin-2 is a nonglycosylated 6.0 kDa disulfide linked heterodimeric protein consisting of a 24 amino acid A-chain and a 29 amino acid B-chain.
Description: IL-2 is a powerful immunoregulatory lymphokine produced by T-cells in response to antigenic or mitogenic stimulation. IL-2/IL-2R signaling is required for T-cell proliferation and other fundamental functions which are essential for the immune response. IL-2 stimulates growth and differentiation of B-cells, NK cells, lymphokine activated killer cells, monocytes, macrophages and oligodendrocytes. Recombinant murine IL-2 is a 17.2 kDa protein, containing 149 amino acid residues.
Description: PAI-2 is an inhibitory serpin expressed mainly in keratinocytes, activated monocytes, and placental trophoblasts. It exists predominantly as a 47 kDa nonglycosylated intracellular protein which can be induced to be secreted as 60 kDa glycoprotein. The glycosylated and unglycosylated forms of PAI-2 are equally effective as inhibitors of urokinase-type plasminogen activator (uPA), the only established physiological target of this serpin. PAI-2 has a unique ability to form dormant polymers spontaneously and reversibly under physiological conditions. The physiological relevance of this property, which is neither a consequence of any mutation in the PAI-2 gene nor associated with any known disorder, is still unclear. However, it appears that the formation of intracellular dormant polymers may be important for the controlled release of the inhibitor from PAI-2 producing cells. Plasma levels of PAI-2 are usually low or undetectable, except during pregnancy and in some forms of monocytic leukemia. Secretion of PAI-2 from the placenta normally occurs during the third trimester of pregnancy and accounts for the dramatic increase in PAI-2 levels (up to 250 ng/ml), which are maintained at these levels until postpartum, and then rapidly decline. In addition to its vital role in protecting the placenta from degradation by uPA and/or uPA-activated proteases, PAI-2 has been shown to be essential for the prevention of metastatic spread of neck, lung and breast cancers. The beneficial effect of PAI-2 seen in these studies is presumed to stem from its ability to inhibit uPA-dependent cell dissemination. PAI-2 has also been reported to inhibit keratinocyte proliferation, and to participate in the innate immune response during viral infection. Recombinant human PAI-2 is a 415-residue nonglycosylated protein.
Description: Matrix metalloproteinases (MMPs) are a family of endoproteases that require zinc and calcium for expressing catalytic activity. These enzymes play a central role in the maintenance and remodeling of the extracellular matrix. Elevated expression of their activity, caused either by up-regulation of their expression or down-regulation of their cognate inhibitors, has been implicated in various degenerative disorders, including arthritis, cardiovascular disease, skeletal growth-plate disorders, and cancer metastasis. MMP-2 is a secreted collagenase with specificity toward Type IV, V, VII, and X collagens. Recombinant human MMP-2 is a 62.0 kDa protein containing the entire catalytic N-terminal domain and the C-terminal domain (552 amino acids).
Description: FGF basic (FGF2) is a multipotential fibroblast growth factor that stimulates and supports proliferation, migration and differentiation. Mouse FGF basic (FGF-2) Recombinant Protein is purified FGF basic (FGF-2) produced in yeast.
Description: Interleukin-2 (IL-2) is a cytokine produced by T-helper cells in response to antigenic or mitogenic stimulation. It is required for T-cell proliferation and other activities crucial to the regulation of the immune response. Chicken IL-2 Recombinant Protein is purified interleukin-2 produced in yeast.
Description: The Trefoil Factor peptides (TFF1, TFF2 and TFF3) are expressed in the gastrointestinal tract, and appear to play an important role in intestinal mucosal defense and repair. TFF2 has been shown to inhibit gastrointestinal motility and gastric acid secretion. Recent data suggests a potential role for TFF2 in acute and chronic asthma (Nikolaidis, N.M. et al. Am. Journal Respir. Cell Mol. Biol. (2003) 4: 458-464). Recombinant human TFF2 is a 12.0 kDa polypeptide of 107 amino acid residues, which includes a 40-amino acid trefoil motif containing three conserved intramolecular disulfide bonds.
Description: ErbB-2 Human Recombinant is a 43.4 kDa protein containing 397 amino acid residues of the human Herstatin, and an extra Methionine at N-Terminal (underlined), produced in E.coli.
Carbon nanothreads allow outstanding enhancement within the thermal conductivity of polyethylene
Polymer nanocomposites with excessive thermal conductivity have been more and more wanted within the digital business. Primarily based on molecular dynamics simulations, this work assesses the thermal transport in polyethylene (PE) nanocomposites with the presence of a brand new one-dimensional nanofiller-a carbon nanothread (NTH). It’s discovered that the axial thermal conductivity of PE nanocomposites will increase linearly with the content material of often aligned NTH fillers, whereas the aggregated sample suppresses the enhancement impact. This phenomenon is defined by a stronger filler-filler interplay that reduces the intrinsic thermal conductivity of the NTH.
Outcomes present that the randomly dispersed NTHs can hardly promote warmth switch as a result of efficient warmth switch channels are missing. Strikingly, floor functionalization has an opposed impact on the thermal conductivity as a result of presence of further voids. The presence of voids solutions a long-standing open query that functionalization of the warmth conductive filler solely barely improves the thermal conductivity of the polymer composite. Moreover, the transverse thermal conductivity degrades within the presence of the NTH and displays no clear correlation with the filler content material or the distribution sample. General, this research gives an in-depth understanding of the warmth switch inside the polymer nanocomposites, which opens up potentialities for the preparation of extremely conductive polymers.
Mixed Remedy With Polyethylene Glycol-20ok and MCC950 Preserves Put up-Resuscitated Myocardial Operate in a Rat Mannequin of Cardiac Arrest and Cardiopulmonary Resuscitation
Background To analyze the therapeutic potential of mixed remedy with polyethylene glycol-20ok (PEG-20ok) and MCC950 on post-resuscitation myocardial operate in a rat mannequin of cardiac arrest. Strategies and Outcomes Thirty rats have been randomized into 5 teams: Sham, Management, PEG-20ok, MCC950, PEG-20ok+ MCC950. Aside from sham, animals have been subjected to six minutes of ventricular fibrillation adopted by eight minutes cardiopulmonary resuscitation. Two milliliters PEG-20ok was administered by intravenous injection coincident with the beginning of cardiopulmonary resuscitation; MCC950 (10 mg/kg), a extremely selective NLRP3 inflammasome inhibitor, was delivered instantly after restoration of spontaneous circulation.
Myocardial operate, sublingual microcirculation, mitochondrial operate, plasma cardiac troponin I, and interleukin-1β, expression of proteins in SIRT1 (sirtuin 1)/PGC-1α (peroxisome proliferator-activated receptor gamma coactivator 1-alpha) and NLRP3 (the NOD-like receptor household protein 3) inflammasome pathways have been evaluated. Following cardiopulmonary resuscitation, myocardial operate was compromised with a considerably decreased cardiac output, ejection fraction, and elevated myocardial efficiency index, cardiac troponin I. Sublingual microcirculation was disturbed with impaired perfused vessel density and microvascular move index.
Cardiac arrest diminished mitochondrial routine respiration, Advanced I-linked respiration, respiratory management charges and oxidative phosphorylation coupling effectivity. PEG-20ok or MCC950 alone restored mitochondrial respiratory operate, restituted sublingual microcirculation, and preserved myocardial operate, whereas a mixture of PEG-20ok and MCC950 additional improved these points. PEG-20ok restored the expression of SIRT1 and PGC-1α, and blunted activation of NLRP3 inflammasomes. MCC950 suppressed expression of cleaved-caspase-1/pro-caspase-1, ASC (apoptosis-associated speck-like protein), GSDMD [gasdermin d], and interleukin-1β.
Conclusions Mixed remedy with PEG-20ok and MCC950 is superior to both remedy alone for preserving post-resuscitated myocardial operate, restituting sublingual microcirculation at restoration of spontaneous circulation at 6 hours. The accountable mechanisms contain upregulated expression of SIRT1/PGC1-α in tandem with inhibition of NLRP3 inflammasomes.
Warmth transport and floor functionalization in nanocomposites of boron nitride nanotubes and polyethylene
This work explores the chance for bettering warmth transport in a polymeric, electrical insulating materials, equivalent to polyethylene, by including boron nitride nanotubes – a warmth superdiffusive materials. We use molecular dynamics simulations to review the nanocomposites fashioned by addition of the nanotubes to each amorphous and crystalline polyethylene, and in addition examine the impact of floor functionalization utilizing a silane coupling agent, which, being covalently hooked up to each the nanofiller and the polymer matrix, facilitates the warmth transport between them.
Though transport is proven to deteriorate in every simulation when the coupling brokers are added, they’re anticipated to favor the nucleation of the crystalline areas in regards to the nanotubes, thus considerably boosting warmth conduction within the materials alongside their course.
EXPRESS: Attenuated Complete ReflectionâFar-Ultraviolet Spectroscopy and Quantum Chemical Calculations of the Digital Construction of the High Floor and Bulk of Polyethylenes with Completely different Crystallinities
On this research, we explored the digital construction of the surfaces of polyethylene samples having completely different crystallinities utilizing attenuated complete reflection (ATR)-far-ultraviolet (FUV) spectroscopy and quantum chemical calculations. Particularly, the ATR-FUV spectra of 5 kinds of high-density polyethylene (HDPE), six kinds of linear low-density PE (LLDPE), and 7 kinds of low-density PE (LDPE) have been obtained. All of the spectra contained an intense band close to 156 nm and a broad band between 180 and 190 nm. Transmission spectra have been obtained for the thin-film (30 μm) PE samples between 165 and 250 nm. On this area, the HDPE movies present very low-intensity bands.
In distinction, the transmission spectra of the LLDPE and LDPE samples yielded weak-to-medium and medium-intensity bands round 180â190 nm, respectively. As well as, to know the variations within the absorption spectra among the many PEs noticed, we simulated the spectra of n-pentane as a PE crystal mannequin utilizing time-dependent density useful concept and located that the frequent intense band at 156 nm is because of the Ï (C(2p)-H)âRydberg 3s, 3p transition. The absorption bands close to 180â190 nm might correspond to aggregates of quite a few molecular chains within the amorphous elements of the LLDPE and LDPE samples.
Binary System of Polyethylene Glycol 200 (1) + 3-Dimethylamino-1-propylamine (2) for CO 2 Absorption: Thermophysical Properties and Spectroscopic Research
Because the focus of CO<sub>2</sub> within the ambiance retains growing, the event of a extremely environment friendly CO<sub>2</sub> absorbent is extremely desired. On this work, a binary combination system of polyethylene glycol 200 (PEG 200) (<b>1</b>) + 3-dimethylamino-propylamine (DMAPA) (<b>2</b>) was used for CO<sub>2</sub> absorption. Contemplating the significance of thermophysical properties to binary options, the densities and viscosities of the PEG 200 (<b>1</b>) + DMAPA (<b>2</b>) combination have been measured at <i>T</i> = (298.15, 303.15, 308.15, 313.15, and 318.15) Ok and atmospheric strain over the whole composition vary. Primarily based on the density and viscosity knowledge, the surplus properties and viscous move thermodynamic parameters have been calculated, respectively.
To acquire the coefficients and to estimate the usual deviations between the experimental and calculated portions, the surplus molar quantity (<i>V</i> <sub>m</sub> <sup>E</sup>), the viscosity deviation (Δη), and the surplus Gibbs free energies of activation for viscous move (Δ<i>G*</i> <sup>E</sup>) have been fitted to the Redlich-Kister equation. Moreover, primarily based on the outcomes of UV-vis, FTIR, and <sup>1</sup>H NMR spectra, the intermolecular interplay of PEG 200 and DMAPA was mentioned. Notably, a robust intermolecular bonding is fashioned when the molar ratio of PEG 200 to DMAPA is about 1:2 due to the surplus molar quantity (<i>V</i> <sub>m</sub> <sup>E</sup>). On that account, a combination of PEG 200 and DMAPA in a ratio of 1:2 was used for finding out CO<sub>2</sub> absorption, and a CO<sub>2</sub> absorption of about 0.19 g per gram of absorbent was achieved at room temperature and ambiance
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
The Intra-assay Precision is determined when 3 samples with low, middle and high level of General Polyethylene Glycol (PEG) were tested on 3 different plates, 8 replicates in each plate
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Description: This is Competitive Enzyme-linked immunosorbent assay for detection of General Polyethylene Glycol (PEG) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
Known also as Polyethylene Glycol elisa. Alternative names of the recognized antigen: PEO
POE
Polyethylene oxide
Polyoxyethylene
Carbowax
GoLYTELY
GlycoLax
Fortrans
TriLyte
Colyte
Halflytely
Macrogol
MiraLAX
MoviPrep
Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of General Polyethylene Glycol (PEG) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids with no significant corss-reactivity with analogues from other species.
A monoclonal antibody specific to Polyethylene Glycol (PEG) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Polyethylene Glycol (PEG) and unlabeled Polyethylene Glycol (PEG) (Standards or sa
Description: A competitive Inhibition ELISA kit for detection of Polyethylene Glycol from General in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
Description: Cannabidiol dimethyl ether (CBDD) is a cannabidiol derivative that potently and selectively inhibits 15-LOX with an IC50 value of 0.28 ?M. 15-LOX can oxygenate cholesterol esters in the low-density lipoprotein (LDL) particle.
Description: Cannabidiol dimethyl ether (CBDD) is a cannabidiol derivative that potently and selectively inhibits 15-LOX with an IC50 value of 0.28 ?M. 15-LOX can oxygenate cholesterol esters in the low-density lipoprotein (LDL) particle.
Description: Cannabidiol dimethyl ether (CBDD) is a cannabidiol derivative that potently and selectively inhibits 15-LOX with an IC50 value of 0.28 ?M. 15-LOX can oxygenate cholesterol esters in the low-density lipoprotein (LDL) particle.
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