138577 Results for: "Air Quality and Atmosphere Activities and Models&"
OneStep™ PCR Inhibitor Removal Kits, Zymo Research
Supplier: Zymo Research
The OneStep™ PCR Inhibitor Removal Kit allows for the efficient removal of contaminants that can inhibit downstream enzymatic reactions from DNA and RNA preparations.
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96-Well PCR Clean-Up Kits, IBI Scientific
Supplier: IBI Scientific
The IBI high throughput 96-Well PCR Clean-Up Kit is designed to recover or concentrate DNA fragments from PCR or other enzymatic reactions using an efficient 96-well binding plate system.
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chemagic Prepito DNA Universal Kit
Supplier: REVVITY HEALTH SCIENCES, INC.
Ready-to-use nucleic acid purification kit to be used with the chemagic Prepito instrument. Based on proprietary M-PVA Magnetic Bead technology. Suitable for diverse sample material, e.g., blood, buffy coat, saliva, plasma, serum, lavage, tissue, cells, DBS, bacterial culture, and amniotic fluid. 180 preps, all plastics included.
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Orion™ Star™ A211 pH Benchtop Meter, Thermo Scientific
Supplier: Thermo Fisher Scientific
Reliably measure pH, mV, ORP, and temperature with the Orion™ Star™ A211 pH Benchtop Meter for advanced lab analysis and printer or computer interfacing.
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Dithiothreitol (DTT, Cleland's reagent) ≥99.5%, white powder for electrophoresis
Supplier: MP Biomedicals
DL-Dithiothreitol is also known as Clelands reagent; Protective agent for sulfhydryl groups (-SH). Quantitatively reduces disulfides (-S-S- to -SH). In this reaction the DTT is oxidized to the cyclic disulfide which ensures the reduction of other disulfides in solution. Disulfide reduction occurs quickly at pH 8.
Dithiothreitol is useful for stabilizing sulfhydryl containing enzymes. Effective in sample buffers for reducing protein disulfide bonds prior to SDS-PAGE. DTT can also be used for reducing the disulfide bridge of the cross-linker N,N'-bis(acryloyl)cystamine to break apart the matrix of a polyacrylamide gel. DTT is less pungent and is less toxic than 2-mercaptoethanol.
Useful for stabilizing sulfhydryl-containing enzymes.
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Anti-ABO Mouse Monoclonal Antibody [clone: HEB-20]
Supplier: Prosci
The antibody HEB-20 reacts with human blood group B. The specificity of the antibody HEB-20 was confirmed by comparison of specificity and reactivity to standard reagent using >5.000 samples of blood. The mAb HEB-20 shows specific staining of erythrocytes and vascular epithelium of blood group B controls and no staining in group A controls. This mAb is applicable for tissue staining in tumor patients with blood groups B and AB. Blood group antigens are generally defined as molecules formed by sequential addition of saccharides to the carbohydrate side chains of lipids and proteins detected on erythrocytes and certain epithelial cells. The A, B and H antigens are reported to undergo modulation during malignant cellular transformation. Blood group related antigens represent a group of carbohydrate determinants carried on both glycolipids and glycoproteins. They are usually mucin type, and are detected on erythrocytes, certain epithelial cells, and in secretions of certain individuals. Sixteen genetically and biosynthetically distinct but inter related specificities belong to this group of antigens, including A, B, H, Lewis A, Lewis B, Lewis X, Lewis Y, and precursor type 1 chain antigens.
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Expression vectors, pGEX
Supplier: Cytiva
The pGEX vectors have an expanded multiple cloning site (MCS) that contains six restriction sites. The expanded MCS facilitates the unidirectional cloning of cDNA inserts obtained from libraries constructed using many available lambda vectors. pGEX-6P-1, pGEX-6P-2, and pGEX-6P-3 each encode the recognition sequence for site-specific cleavage by PreScission Protease between the GST domain and the multiple cloning site. pGEX-4T-1, pGEX-4T-2, and pGEX-4T-3 are derived from pGEX-2T and contain a Thrombin recognition site. pGEX-5X-1, pGEX-5X-2, and pGEX5X-3 are derivatives of pGEX-3X and possess a Factor Xa recognition site.
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ANTIBODY 5-CARBOXYLCYTOSINE 5-CAC PAB
Supplier: Active Motif
ANTIBODY 5-CARBOXYLCYTOSINE 5-CAC PAB
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ANTIBODY ANDROGEN RECEPTOR 100UL
Supplier: Active Motif
ANTIBODY ANDROGEN RECEPTOR 100UL
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RECOMBINANT NUCLEOSOMES (H3.1)
Supplier: Active Motif
RECOMBINANT NUCLEOSOMES (H3.1)
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CHROMATIN IMMUNOPRECIPITATION KIT
Supplier: Active Motif
CHROMATIN IMMUNOPRECIPITATION KIT
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RECOMBINANT TET2 1129-2002 PROTEIN
Supplier: Active Motif
RECOMBINANT TET2 1129-2002 PROTEIN
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CHARIOT PROTEIN DELIVERY REAGENT 25RXN
Supplier: Active Motif
CHARIOT PROTEIN DELIVERY REAGENT 25RXN
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ANTIBODY 5-FORMYLCYTOSINE 5-FC PAB 10UL
Supplier: Active Motif
ANTIBODY 5-FORMYLCYTOSINE 5-FC PAB 10UL
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ANTIBODY HISTONE H3K36ME3 (PAB) 100UG
Supplier: Active Motif
ANTIBODY HISTONE H3K36ME3 (PAB) 100UG
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ANTIBODY HISTONE H3K36ME1 (PAB) 100UL
Supplier: Active Motif
ANTIBODY HISTONE H3K36ME1 (PAB) 100UL
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ANTIBODY HISTONE H3K36ME2 (PAB) 200UL
Supplier: Active Motif
ANTIBODY HISTONE H3K36ME2 (PAB) 200UL
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Wizard Plus SV Minipreps Start-Up Kit, 110 V Electrical (750 preps, Manifold and Free Vacuum Pump), 1 each, Promega
Supplier: Promega Corporation
Bundle of 750 minipreps, vacuum manifold and free vacuum pump. Wizard Plus SV Minipreps is silica membrane-based system for simple, rapid isolation of plasmid DNA from 1-10ml E. coli cultures in 45 minutes or less.
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Zymoclean™, Gel RNA Recovery Kit, Zymo Research
Supplier: Zymo Research
The Zymoclean™ Gel RNA Recovery Kit provides a quick purification method for recovery of RNA fragments from agarose gels.
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E.Z.N.A.® RNA Isolation Kits, Omega Bio-Tek
Supplier: Omega Bio-Tek
Isolated RNA can be used for Northern blotting, RT-PCR, nuclease protection assays, in vitro translation, and microarray analysis
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Mag-Bind® Fit24™ cfDNA Kit
Supplier: Omega Bio-Tek
Pre-scripted solution for the purification of cfDNA from up to 4 ml plasma samples.
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ANTIBODY HISTONE H3K36ME3 (MAB) 100UG
Supplier: Active Motif
ANTIBODY HISTONE H3K36ME3 (MAB) 100UG
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Anti-CABC1 Rabbit Polyclonal Antibody
Supplier: Bioss
May be a chaperone-like protein essential for the proper conformation and functioning of protein complexes in the respiratory chain.Tissue specificity:Ubiquitously expressed with a relatively greater abundance in heart and skeletal muscle.Involvement in disease:Defects in ADCK3 are a cause of coenzyme Q10 deficiency (CoQ10 deficiency). CoQ10 deficiency is an autosomal recessive disorder with variable manifestations. It can be associated with three main clinical phenotypes: a predominantly myopathic form with central nervous system involvement, an infantile encephalomyopathy with renal dysfunction and an ataxic form with cerebellar atrophy.Defects in ADCK3 are the cause of spinocerebellar ataxia autosomal recessive type 9 (SCAR9) [MIM:612016]; also known as autosomal recessive cerebellar ataxia type 2 (ARCA2). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR9 is an autosomal recessive form characterized by gait ataxia and cerebellar atrophy with slow progression and few associated features. Patients can manifest brisk tendon reflexes and Hoffmann sign, mild psychomotor retardation, mild axonal degeneration of the sural nerve, exercise intolerance and elevated serum lactate.
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Anti-CABC1 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
May be a chaperone-like protein essential for the proper conformation and functioning of protein complexes in the respiratory chain.Tissue specificity:Ubiquitously expressed with a relatively greater abundance in heart and skeletal muscle.Involvement in disease:Defects in ADCK3 are a cause of coenzyme Q10 deficiency (CoQ10 deficiency). CoQ10 deficiency is an autosomal recessive disorder with variable manifestations. It can be associated with three main clinical phenotypes: a predominantly myopathic form with central nervous system involvement, an infantile encephalomyopathy with renal dysfunction and an ataxic form with cerebellar atrophy.Defects in ADCK3 are the cause of spinocerebellar ataxia autosomal recessive type 9 (SCAR9) [MIM:612016]; also known as autosomal recessive cerebellar ataxia type 2 (ARCA2). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR9 is an autosomal recessive form characterized by gait ataxia and cerebellar atrophy with slow progression and few associated features. Patients can manifest brisk tendon reflexes and Hoffmann sign, mild psychomotor retardation, mild axonal degeneration of the sural nerve, exercise intolerance and elevated serum lactate.
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ANTIBODY MAB H3K27ME2ME3 10UL
Supplier: Active Motif
ANTIBODY MAB H3K27ME2ME3 10UL