Apotex Pharmachem Pharmaceutical Purity Ingredients Distributor CAS numbers MSDS
cadmium elimination from aqueous resolution by Enteromorpha prolifera
Mechanism of an Elusive Solvent Impact in Organozinc Reagent Synthesis.
Solvent results are sometimes obscure in instances the place response intermediates, and thus their differential behaviour in numerous solvents, usually are not instantly observable by conventional ensemble analytical methods. Herein, the sensitivity of single-particle fluorescence microscopy uniquely permits direct remark of organozinc intermediates and solvent results on their build-up and persistence.
When mixed with NMR spectroscopy, these imaging information pinpoint the beforehand elusive mechanistic origin of solvent results within the synthesis of broadly used organozinc reagents. These findings characterize the acceleration of oxidative addition of the beginning organoiodide to the floor of zinc steel in DMSO relative to THF, however as soon as fashioned, floor intermediates show comparable persistence in both solvent. The present research are the primary demonstration of a extremely delicate, single-particle fluorescence microscopy method to pinpoint in any other case elusive solvent results in artificial chemistry.
The Significance of Derivatizing Reagent in Chromatography Purposes for Biogenic Amine Detection in Meals and Drinks.
Biogenic amines (BA) are chemical compounds fashioned in meals that include protein, permitting the meals to endure a bacterial degradation course of. Biogenic amines are labeled as poisonous meals as a result of its consumption exceeding the FDA regulation (50 mg/kg) could be dangerous to people. Some nations even have laws that prohibit the consumption of biogenic amines in excessive concentrations, particularly histamine.
The chromatography strategies typically utilized by researchers are liquid chromatography (LC) and gasoline chromatography (GC), the place using a derivatization reagent is critical to extend their sensitivity. This evaluate relies on previous and current research about biogenic amine detection associated to meals samples. The rationale of this research can also be to offer information on the comparability of the analytical approaches between LC and GC strategies. Moreover, the assorted approaches of biogenic amine dedication and probably the most utilized analytical strategies have been reviewed.
Description: Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. The function of the fiber cell membrane protein encoded by this gene is undetermined, yet this protein is speculated to play a role in intracellular communication. The MIP protein is expressed in the ocular lens and is required for correct lens function. This gene has been mapped among aquaporins AQP2, AQP5, and AQP6, in a potential gene cluster at 12q13.
Description: MIP-3 is a CC chemokine that signals through the CCR1 receptor. MIP-3 chemoattracts monocytes, resting T-lymphocytes and neutrophils, but does not chemoattract activated lymphocytes. Additionally, MIP-3 has been shown to inhibit colony formation of bone marrow myeloid immature progenitors. Recombinant human MIP-3 is an 11.3 kDa protein containing 99 amino acid residues, including the four highly conserved cysteine residues present in CC chemokines.
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-3 degrades fibronectin, laminin, collagens III, IV, and X, and cartilage proteoglycans. Recombinant human MMP-3 is a 42.8 kDa protein containing the entire catalytic N-terminal domain and the C-terminal domain (378 amino acids).
IL-3 Interleukin-3 Human Recombinant Protein, His Tag
Description: Interleukin-3 Human Recombinant produced in E.Coli is single, a non-glycosylated, Polypeptide chain containing 154 amino acids fragment (20-152) and having a total molecular mass of 17.3kDa and fused with a 20 aa N-terminal His tag. ;The IL3 His is purified by proprietary chromatographic techniques.
Description: MIP-3α is a CC chemokine that is expressed in the liver, lymph nodes, appendix, PBL and lung and can signal through the CCR6 receptor. MIP-3α is chemotactic towards lymphocytes and dendritic cells. Additionally, it promotes the adhesion of memory CD4+ T cells and inhibits colony formation of bone marrow myeloid immature progenitors. Recombinant human MIP-3α is an 8.0 kDa protein containing 70 amino acid residues, including the four highly conserved cysteine residues present in CC chemokines.
Description: MIP-3β is a CC chemokine that is expressed in the thymus, lymph nodes and in activated bone marrow stromal cells and signals through the CCR7 receptor. MIP-3β is a chemoattractant for T and B lymphocytes and myeloid progenitor cells. Human MIP-3β is active on murine cells. Recombinant human MIP-3β is an 8.8 kDa protein containing 77 amino acid residues, including the four highly conserved cysteine residues present in CC chemokines.
Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against MIP. Recognizes MIP from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.ELISA:1/5000
Description: A polyclonal antibody against MIP. Recognizes MIP from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:2000-1:5000, IHC:1:20-1:100
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against mip. Recognizes mip from Legionella pneumophila. This antibody is Unconjugated. Tested in the following application: ELISA
Description: A polyclonal antibody against MIP. Recognizes MIP from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:1000-1:5000, IHC:1:50-1:200
Description: A polyclonal antibody against MIP. Recognizes MIP from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:500-1:5000, IHC:1:50-1:200
Description: A polyclonal antibody against MIP. Recognizes MIP from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC;ELISA:1:1000-1:5000, IHC:1:50-1:200
Description: A polyclonal antibody against MIP. Recognizes MIP from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB
Buffer: Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against MIP. Recognizes MIP from Human. This antibody is Unconjugated. Tested in the following application: ELISA, IHC, IF; Recommended dilution: IHC:1:200-1:500, IF:1:50-1:200
Description: Rabbit Monoclonal Thyroglobulin Antibody. Validated in IF, WB and tested in Human, Mouse, Rat.
Comparative analysis of nucleic acid stabilizing reagents for RNA- and DNA-based Leishmania detection in blood as proxy for visceral burdens.
Molecular detection methods utilizing peripheral blood are most popular over invasive tissue aspiration for the prognosis and post-treatment follow-up of visceral leishmaniasis (VL) sufferers. This research goals to establish appropriate stabilizing reagents to forestall DNA and RNA degradation throughout storage and transport to specialised laboratories the place molecular prognosis is carried out.
The stabilizing capacities of various commercially accessible reagents have been in contrast utilizing promastigote-spiked human blood and peripheral blood of Syrian golden hamsters subjected to experimental an infection, therapy (miltefosine of aminopyrazole DNDi-1044) and immunosuppression.
The affect of assorted storage temperature circumstances was examined together with a longtime kinetoplast DNA (kDNA) qPCR and a lately developed spliced chief RNA (SL-RNA) assay for Leishmania detection.Regardless of the blood sort and stabilizer used, threshold (cT) values obtained with the SL-RNA qPCR have been systematically decrease than these obtained with the kDNA assay, confirming the benefit of the SL-RNA assay over the broadly used kDNA assay for low-level Leishmania detection. Peripheral blood parasite ranges correlated comparatively nicely with hepatic burdens. RNA Shield Cell Reagent offered probably the most optimum simultaneous DNA and RNA stabilization in each human and hamster blood.
Nonetheless, this stabilizer requires an erythrocyte lysis step, which could be difficult underneath discipline circumstances. DNA/RNA Protect gives a superb various for downstream kDNA and SL-RNA assays, particularly if pattern storage capability at 4 °C could be assured.The really useful stabilizing reagents are suitable with RNA- and DNA-based Leishmania detection in peripheral blood within the VL hamster mannequin and spiked human blood. Since molecular detection methods utilizing peripheral blood are much less invasive than microscopic evaluation of tissue aspirates, the findings of this research could also be utilized to human VL medical research.
Comparability of adsorption properties for cadmium elimination from aqueous resolution by Enteromorpha prolifera biochar modified with completely different chemical reagents.
Utilizing biochar to take away heavy metals from water is environmentally helpful. On this research, three sorts of chemical reagents, together with ZnCl2, H3PO4 and KMnO4, have been launched to switch the biochar derived from Enteromorpha prolifera. The efficiency of those modified biochar in eradicating Cadmium ions (Cd(II)) from water was investigated. The physicochemical properties of activated biochars have been characterised by N2-sorption, thermal gravity and differential thermal gravity (TG/DTG), scanning electron microscopy (SEM), elemental evaluation and Fourier remodel infrared spectroscopy (FTIR).
The outcomes confirmed that the elimination price of Cd(II) from water by EP biochar modified with H3PO4 was considerably elevated, and the utmost adsorption capability of Cd(II) reached to 423 mg/g for PBC. Furthermore, the adsorption of Cd(II) from water by phosphoric acid modified biochar was very quick, and the saturation adsorption of Cd(II) was reached inside 1 h.
In contrast with pseudo first-order mannequin, pseudo secondary-order mannequin was way more appropriate for analyzing the adsorption kinetics information of Cd(II) onto KBC or ZBC. The adsorption of Cd(II) onto PBC was analyzed by the intra-particle diffusion kinetic mannequin, the place the worth of R2 was excessive as 0.98. The Langmuir mannequin was match for phosphoric acid modified biochar.
Should the Human Neurotensin (NT) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Human Neurotensin (NT) in samples from serum, plasma or other biological fluids.
Should the Human Neurotensin (NT) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Human Neurotensin (NT) in samples from serum, plasma or other biological fluids.
Should the Nitrotyrosine (NT) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Nitrotyrosine (NT) in samples from serum, plasma, tissue homogenates or other biological fluids.
Should the Nitrotyrosine (NT) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Nitrotyrosine (NT) in samples from serum, plasma, tissue homogenates or other biological fluids.
Description: NT-4 is a neurotrophic factor structurally related to β-NGF, BDNF, and NT-3. These proteins belong to the cysteine-knot family of growth factors that assume stable dimeric structures. NT-4 is expressed in the prostate, thymus, placenta and skeletal muscle. NT-4 can signal through the LNGFR and trkB receptors and promotes the survival of peripheral sensory sympathetic neurons. Recombinant human NT-4 is a noncovalently linked homodimer, of two 14.0 kDa polypeptide monomers (260 total amino acid residues).
Should the Rat Neurotensin (NT) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Rat Neurotensin (NT) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Should the Rat Neurotensin (NT) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Rat Neurotensin (NT) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Description: Quantitativesandwich ELISA kit for measuring Human Neurotrophin 4, NT-4 in samples from serum, plasma, cell culture supernates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Human Neurotrophin 4, NT-4 in samples from serum, plasma, cell culture supernates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Neurotrophin-4 Human Recombinant produced in E.Coli is a noncovalently linked homodimer, non-glycosylated polypeptide chain containing 2 x 130 amino acids (81-210 amino acids) and having a total molecular mass of 28 kDa. ;The NT-4 is purified by proprietary chromatographic techniques.
Immunogen information: Synthesized peptide derived from the Internal region of human NT-4
Applications tips:
Description: A polyclonal antibody for detection of NT-4 from Human, Mouse, Rat. This NT-4 antibody is for IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human NT-4
Immunogen information: Synthesized peptide derived from the Internal region of human NT-4
Applications tips:
Description: A polyclonal antibody for detection of NT-4 from Human, Mouse, Rat. This NT-4 antibody is for IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human NT-4
Immunogen information: Synthesized peptide derived from the Internal region of human NT-4
Applications tips:
Description: A polyclonal antibody for detection of NT-4 from Human, Mouse, Rat. This NT-4 antibody is for IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the Internal region of human NT-4
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human NT-4 . This antibody is tested and proven to work in the following applications:
Gentaur's NT-4 CLIA kit utilizes the Sandwich- CLIA principle. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Human NT-4 . Standards or samples are added to the micro CLIA plate wells and combined with the
Gentaur's NT-4 ELISA kit utilizes the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human NT-4. Standards or samples are added to the micro ELISA plate wells and combined with th
Description: Interleukin-4 Human Recombinant produced in yeast is a single, glycosylated polypeptide chain containing 129 amino acids.;The IL-4 is purified by proprietary chromatographic techniques.
Description: Quantitativesandwich ELISA kit for measuring Mouse Neurotrophin 4, NT-4 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Mouse Neurotrophin 4, NT-4 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativesandwich ELISA kit for measuring Rat Neurotrophin 4, NT-4 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Rat Neurotrophin 4, NT-4 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: 4-1BB Receptor, a member of the TNF superfamily of receptors, is mainly expressed on the surface of a variety of T cells, but also found in B cells, monocytes, and various transformed cell lines. 4-1BB Receptor binds to 4-1BBL to provide a co-stimulatory signal for T lymphocytes. Signaling by 4-1BB Receptor has been implicated in the antigen-presentation process and generation of cytotoxic T cells. The human 4-1BB Receptor gene codes for a 255 amino acid type I transmembrane protein containing a 17 amino acid N-terminal signal sequence, a 169 amino acid extracellular domain, a 27 amino acid transmembrane domain and a 42 amino acid cytoplasmic domain. Recombinant human soluble 4-1BB Receptor is a 167 amino acid polypeptide (17.7 kDa), which contains the cysteine rich TNFR-like extracellular domain of 4-1BB Receptor.
Description: PF-4 is a CXC chemokine that is expressed in megakaryocytes and stored in the α-granules of platelets. PF-4 is chemotactic towards neutrophils and monocytes and has been shown to inhibit angiogenesis. Recombinant human PF-4 is a 7.8 kDa protein containing 70 amino acid residues, including the four highly conserved residues present in CXC chemokines.
Description: The plasma concentrations of both the N-terminal fragment of Pro-B-type natriuretic peptide (NT-proBNP) and prohormone of brain natriuretic peptide (proBNP) are significantly increased in patients with asymptomatic and symptomatic left ventricular dysfunction.
Description: The plasma concentrations of both the N-terminal fragment of Pro-B-type natriuretic peptide (NT-proBNP) and prohormone of brain natriuretic peptide (proBNP) are significantly increased in patients with asymptomatic and symptomatic left ventricular dysfunction.
Description: NT-3 is a protein encoded by the NTF3 gene which is approximately 29,4 kDa. NT-3 is secreted and is involved in apoptotic pathways in synovial fibroblasts, the GPCR pathway, ERK signalling, TGF-beta pathway and nanog in mammalian ESC pluripotency. This protein falls under the neurotrophin family. It controls survival and differentiation of mammalian neurons and is closely related to both nerve growth factor and brain-derived neurotrophic factor. It may be involved in the maintenance of the adult nervous system, and may affect development of neurons in the embryo. NT-3 is expressed in the brain and peripheral tissues. Mutations in the NTF3 gene result in diabetic neuropathy and pediatric fibrosarcoma. STJ98718 was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen. This polyclonal antibody binds to endogenous NT-3.
Gentaur's NT-4 CLIA kit utilizes the Sandwich- CLIA principle. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Mouse NT-4 . Standards or samples are added to the micro CLIA plate wells and combined with the
Gentaur's NT-4 CLIA kit utilizes the Sandwich- CLIA principle. The micro CLIA plate provided in this kit has been pre-coated with an antibody specific to Rat NT-4 . Standards or samples are added to the micro CLIA plate wells and combined with the sp
Gentaur's NT-4 ELISA kit utilizes the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Mouse NT-4. Standards or samples are added to the micro ELISA plate wells and combined with th
Gentaur's NT-4 ELISA kit utilizes the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat NT-4. Standards or samples are added to the micro ELISA plate wells and combined with the
Should the Human N-Terminal Pro Atrial Natriuretic Peptide (NT-ProANP) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human N-Terminal Pro Atrial Natriuretic Peptide (NT-ProANP) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Human N-Terminal Pro Atrial Natriuretic Peptide (NT-ProANP) ELISA Kit
Should the Human N-Terminal Pro Atrial Natriuretic Peptide (NT-ProANP) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human N-Terminal Pro Atrial Natriuretic Peptide (NT-ProANP) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Human N-Terminal Pro Brain Natriuretic Peptide (NT-ProBNP) ELISA Kit
Should the Human N-Terminal Pro Brain Natriuretic Peptide (NT-ProBNP) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human N-Terminal Pro Brain Natriuretic Peptide (NT-ProBNP) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Human N-Terminal Pro Brain Natriuretic Peptide (NT-ProBNP) ELISA Kit
Should the Human N-Terminal Pro Brain Natriuretic Peptide (NT-ProBNP) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human N-Terminal Pro Brain Natriuretic Peptide (NT-ProBNP) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Human N-Terminal Pro Atrial Natriuretic Peptide (NT-ProANP) ELISA Kit
Should the Human N-Terminal Pro C-Type Natriuretic Peptide (NT-ProCNP) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Human N-Terminal Pro C-Type Natriuretic Peptide (NT-ProCNP) in samples from serum, plasma, tissue homogenates or other biological fluids.
Human N-Terminal Pro C-Type Natriuretic Peptide (NT-ProCNP) ELISA Kit
Should the Human N-Terminal Pro C-Type Natriuretic Peptide (NT-ProCNP) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A competitive inhibition quantitative ELISA assay kit for detection of Human N-Terminal Pro C-Type Natriuretic Peptide (NT-ProCNP) in samples from serum, plasma, tissue homogenates or other biological fluids.
Human N-Terminal Pro C-Type Natriuretic Peptide (NT-ProCNP) ELISA Kit
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