Additional Selective and Differential Cell Culture Media
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Filtered Search Results
Bioworld Murashige and Skoog(MS) Medium, Modification No. 2, 50 L
Murashige & Skoog (MS) MediumContains Micronutrients and 3/4 Macronutrients as described by Murashige & Skoog (1967) Sucrose, Cytokines, Vitamins, and Auxins should be added as needed Provided as 1 unit to make 10L, 25L, or 50L of medium, or as 10 units to make 1L of medium Plant tissue culture tested
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Bioworld Knudson C Orchid Medium, Morel Modification, 25 L
Knudson C Orchid MediumContains Macronutrients, Micronutrients, and Sucrose as described by Knudson (1946) Cytokines, Vitamins, and Auxins should be added as needed Provided as 1 unit to make 10L, 25L, or 50L of medium, or as 10 units to make 1L of mediumPlant tissue culture testedWorking Concentration: 22.0 g/LpH: 4.0−5.0Soluble in water
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Research Products International Corp Nutrient Broth, 5 Kilograms
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For cultivating a variety of non-fastidious organisms.
Dissolve 8 grams in one liter distilled water. Heat solution to boiling with continuous stirring for one minute. Sterilize by autoclaving at 121°C for 15 minutes. Store at room temperature.
Beef Extract: 3 g/l
Pancreatic Digest of Gelatin: 5 g/l
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Sigma Aldrich Fine Chemicals Biosciences Endothelial Cell Growth Me
Endothelial Cell Growth Medium 2 Kit
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ATHENA ES DMEM Low Glucose
Dulbecco's Modified Eagle Medium (DMEM) is a widely used basal medium for supporting the growth of many different mammalian cells. Cells successfully cultured in DMEM include primary fibroblasts, neurons, glial cells, HUVECs, and smooth muscle cells, as well as cell lines such as HeLa, 293, Cos-7, and PC-12. Dulbecco's Modified Eagle Medium (DMEM) is modified to contain four times the amino acid and vitamin concentration of original Eagle's Minimal Essential Medium. Like the original DMEM formulation, this formulation contains a low concentration of glucose (1 g/L). DMEM also uses a sodium bicarbonate buffer system, allowing for maintenance of physiological pH in a 5–10% CO2 environment. Importantly, DMEM commonly requires fetal bovine serum (FBS) supplementation.
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ATHENA ES VALI Medium
VALI (Vertex modified Air-Liquid Interface) medium is derived from ALI medium. The VALI version was developed to support drug-discovery using human bronchial epithelial cells in an air-liquid surface model
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American Research Products Inc BoVine Epithelial growth facto
BoVine Epithelial growth factor (EGF) ELISA Kit from CUSABIO Detection Range 0 156 ng/mL-10 ng/mL Sensitivity 0 039 ng/mL Sample serum plasma Method Sandwich
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ATCC HS 739.T HUMAN FIBROBLAST CELL
HS 739 T HUMAN FIBROBLAST CELL
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New England Biolabs, Inc. Yeast Medium Pack – 12 g
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The Yeast Carbon Base Medium Powder contains sufficient reagents needed to make 1 liter of Yeast Carbon Base (YCB) Agar Medium containing 5 mM acetamide. YCB Agar Medium is used for acetamide selection of K. lactis cells that have been transformed with a pKLAC1-based expression vector (NEB #N3740).
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NEOGEN Lauryl Sulfate Broth, 10 kg
Lauryl Sulfate Broth is used for the detection of coliform bacteria in water and wastewater in a laboratory setting. Lauryl Sulfate Broth is not intended for use in the diagnosis of disease or other conditions in humans.The coliform group of bacteria includes aerobic and facultative anaerobic, Gram-negative, non-sporeforming bacilli that ferment lactose and form acid and gas at 35°C within 48 hours. Members of the Enterobacteriacae comprise the majority of this group, but organisms such as Aeromonas spp. may also be included. Procedures to detect and confirm coliforms are used in testing water, foods, dairy products, and other materials.Lauryl Sulfate Broth, also referred to as Lauryl Tryptose Broth, is prepared according to the formula of Mallmann and Darby. During their investigation, Sodium Lauryl Sulfate produced the best results for inhibition of organisms other than coliforms. For more information visit https://www.neogen.com/solutions/Microbiology/lauryl-sulfate-broth
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Cell Applications Inc Rat Neuron Plating Solution I
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Rat Neuron Plating Solution I
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NEOGEN Malt Extract, 500 g
Malt Extract is a dehydrated extract of malt for use in preparing microbiological culture media in a laboratory setting. Malt Extract is not intended for use in the diagnosis of disease or other conditions in humans.Malt Extract is a clarified, water-soluble extract of malted barley. Malt Extract is a useful ingredient of culture media designed for the propagation of yeasts and molds. This ingredient is suitable for yeasts and molds because it contains a high concentration of carbohydrates, particularly maltose. The approximate percentage of reducing sugars in Malt Extract is 60 – 63%.The high carbohydrate content makes malt extract very sensitive to overheating which results in darkening of the medium it is used in. Malt Extract is generally employed in culture media at concentrations between 10 to 100 grams per liter.For more information visit https://www.neogen.com/solutions/Microbiology/malt-extract
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Bioworld Murashige and Skoog (MS) Medium w/ Modified Vitamins, 50 L
Murashige & Skoog (MS) MediumContains Macronutrients, Micronutrients, and Modified Vitamins as described by Murashige & Skoog (1967)Sucrose, Cytokines, and Auxins should be added as needed Provided as 1 unit to make 10L, 25L, or 50L of mediumPlant tissue culture tested
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Bioworld Linsmaier and Skoog Vitamin Mix, 100 mL
Linsmaier & Skoog Vitamin MixContains the Vitamins as described by Linsmaier & Skoog (1965)Package contains 10.04 g vitamins to prepare 100 mL of 1000X vitamin stock solution Use 1 mL per liter of mediumContents: myo-Inositol 100.00 mg/L Thiamine HCl 0.40 mg/L
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NEOGEN Schaedler Agar, 500 g
Schaedler Agar is used for the cultivation of anaerobic microorganisms in a laboratory setting. Schaedler Agar is not intended for use in the diagnosis of disease or other conditions in humans. Survival of anaerobic bacteria is dependent on their sensitivity to oxygen, nutritional requirements, appropriate collection, culture medium, and incubation time and temperature. Schaedler Agar is suitable for standard procedures used in cultivating anaerobic bacteria. Schaedler Agar is prepared according to the formulation described by Schaedler, Dubos, and Costello, and modified by Mata, Carrillo, and Villatoro. Modifications include reduced dextrose to avoid interference with hemolytic reactions, reduced yeast extract to avoid darkening of the medium, and adjusted sodium chloride and nitrogen concentrations.For more information visit https://www.neogen.com/solutions/Microbiology/schaedler-agar
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