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Apexbio Technology LLC HyperTrap SP HP Column 5x1ml
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HyperTrap SP HP Column is a chromatography medium designed for the efficient purification of biomolecules based on strong cation exchange principles The column utilizes sulfopropyl (SP) ligands immobilized on a high-performance matrix allowing selective binding of positively charged proteins and peptides under controlled buffer conditions This mechanism facilitates the separation and enrichment of target analytes from complex biological samples The HyperTrap SP HP Column is commonly applied in protein purification workflows biomarker discovery and quality control assays within biomedical research
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BIOHIPPO AAV-HypoCretin-GCaMP6s-WPRE-pA
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Recombinant adeno associated virus expressing GCaMP6s under the HypoCretin promoter with WPRE and hGH polyA elements. The Cre dependent configuration enables expression only after recombination, providing precise targeted control of targeted neurons. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
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Medchemexpress LLC DIMETHYLPROPIOTHETIN 25G
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5000206810 DIMETHYLPROPIOTHETIN 25G
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Medchemexpress LLC Ecotin E. coli His 100ug | 100ug
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Ecotin a bacterial protein inhibitor regulates serine proteases like trypsin and subtilisin Ecotin s unique surface loop forms a stable complex influencing enzymatic activity Ecotin Protein E coli (His) is the recombinant E coli-derived Ecotin protein expressed by E coli with C-His labeled tag
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Medchemexpress LLC ADAMTS13 HUMAN CHO 5UG
5000194966 ADAMTS13 HUMAN CHO 5UG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000343072 AZD-8835 25MG
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eMolecules EMOLECULES INC
5000474201 BIS TRISTERT-BUTYLPHOSPHI 1G
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eMolecules 2-BROMO PHENOL | AstaTech | 95-56-7 | MFCD00002146 | 173.009 | C6H5BrO | 95.000 | Oc1ccccc1Br | 25g | 206677456
2-BROMO PHENOL | AstaTech | 95-56-7 | MFCD00002146 | 173.009 | C6H5BrO | 95.000 | Oc1ccccc1Br | 25g | 206677456
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Medchemexpress LLC MEDCHEMEXPRESS LLC
5000432493 SULFAMETHAZINE SODI 5G
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Apexbio Technology LLC Difloxacin HCl 91296-86-5 10mM (in 1mL DMSO)
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Difloxacin HCl (CAS 91296-86-5) is a small-molecule inhibitor targeting DNA gyrase and topoisomerase IV It is designed to interfere with DNA gyrase-mediated DNA synthesis thereby inhibiting bacterial DNA replication and cell division Difloxacin HCl exerts its biological activity primarily through inhibition of DNA gyrase and topoisomerase IV In cultured human neuroblastoma cells exhibiting multidrug resistance associated protein (MRP)-mediated chemoresistance difloxacin HCl (50 g/ml) increases cell sensitivity to MRP substrates including doxorubicin vincristine daunorubicin and potassium antimony tartrate indicating reversal of the drug-resistance phenotype Based on these pharmacological properties difloxacin HCl holds research potential in antimicrobial susceptibility testing and studies of multidrug resistance reversal
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Apexbio Technology LLC HATU 148893-10-1 500g
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HATU (1-[Bis(dimethylamino)methylene]-1H-1 2 3-triazolo[4 5-b]pyridinium 3-oxid hexafluorophosphate) is a peptide coupling reagent routinely employed for amide-bond formation in peptide synthesis and other biomolecular applications In solution HATU converts carboxylic acids into active ester intermediates (OAt esters) facilitating subsequent nucleophilic attack from amines or alcohols This reaction typically proceeds in presence of basic additives such as N N-Diisopropylethylamine (DIPEA) under anhydrous conditions in solvents like dimethylformamide (DMF) Its utility extends to synthesizing peptides and modifying biomolecules through ester or amide linkage formation widely applied in biomedical research and pharmaceutical laboratories
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Medchemexpress LLC Triethylmethylammoni 100g
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Triethylmethylammonium chloride is a quaternary ammonium salt belonging to the class of alkylammonium salts This compound is widely used as a phase transfer catalyst in organic synthesis to facilitate the transfer of reactants between immiscible phases In addition it can be used as an electrolyte in electrochemical devices a surfactant in emulsion polymerization and a corrosion inhibitor Its unique chemical properties make it an important ingredient in a variety of industrial applications including pharmaceuticals agrochemicals and materials science
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Medchemexpress LLC Galaxolide 100g
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Galaxolide can induce estrogenic activity (Estrogen Receptor/ERR) trigger oxidative stress and genotoxicity and induce EROD and GST (Glutathione S-transferase) enzyme activity[1][2]
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Apexbio Technology LLC PTP Inhibitor I 2491-38-5 50g
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PTP Inhibitor I (CAS 2491-38-5) is a small molecule inhibitor targeting protein tyrosine phosphatases (PTPs) specifically SHP-1 and PTP1B with inhibition constants (KI) of 43 M and 42 M respectively As an -bromoacetophenone derivative it acts as a neutral phosphotyrosine mimetic covalently modifying the active site cysteine of PTPs Structure-activity studies indicate that modifications to the phenyl ring moderately affect potency while para-substituted peptidyl groups can enhance both potency and selectivity PTP Inhibitor I is utilized in vitro for mechanistic studies of PTP function related to diabetes neurodegenerative disorders immune regulation and pathogen virulence Animal and clinical data are not available
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Apexbio Technology LLC PTP Inhibitor I 2491-38-5 5g
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PTP Inhibitor I (CAS 2491-38-5) is a small molecule inhibitor targeting protein tyrosine phosphatases (PTPs) specifically SHP-1 and PTP1B with inhibition constants (KI) of 43 M and 42 M respectively As an -bromoacetophenone derivative it acts as a neutral phosphotyrosine mimetic covalently modifying the active site cysteine of PTPs Structure-activity studies indicate that modifications to the phenyl ring moderately affect potency while para-substituted peptidyl groups can enhance both potency and selectivity PTP Inhibitor I is utilized in vitro for mechanistic studies of PTP function related to diabetes neurodegenerative disorders immune regulation and pathogen virulence Animal and clinical data are not available
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