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Image Unavailable-EDVO270

Experimentation kits, antigen-antibody interaction: the ouchterlony procedure

Catalog Number: (EDVO270)
Supplier: EDVOTEK
Description: This experiment introduces students to the principles of antigen-antibody interactions by using the Ouchterlony procedure. Antibodies and antigens form complexes that precipitate, making it possible to assay antibody-antigen systems. The binding interaction results in the formation of a white precipitate after diffusion in agarose.
UOM: 1 * 1 items
Product Image-EDVO207

Experimentation kits, southern blot analysis

Catalog Number: (EDVO207)
Supplier: EDVOTEK
Description: This experiment introduces students to Southern blotting as a tool for DNA fingerprinting in a hypothetical paternity determination. DNA fragments are first separated by agarose gel electrophoresis, then transferred to a nylon membrane and finally visualised by staining.
UOM: 1 * 1 items
Image Unavailable-BOSSBS-13390R-CY3

Anti-GLUD2 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-13390R-CY3)
Supplier: Bioss
Description: GLUD2 is both mitochondrial matrix enzymes belonging to the Glu/Leu/Phe/Val dehydrogenases family. Exisiting as homohexamers, GLUD1 catalyzes the oxidative deamination of glutamate to ?ketoglutarate and ammonia while GLUD2 is involved in the recycling of glutamate during neurotransmission. GLUD1 is critical for regulating amino acid induced insulin secretion and is allosterically activated by ADP and inhibited by GTP and ATP. Mutations in the gene encoding GLUD1 causes hyperinsulinism-hyperammonemia syndrome (HHS), which is an inherited condition characterized by high insulin and ammonia levels in the blood. GLUD1 may also be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate. GLUD2 is expressed in testis and retina, with lower levels found in brain.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13390R-CY5

Anti-GLUD2 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-13390R-CY5)
Supplier: Bioss
Description: GLUD2 is both mitochondrial matrix enzymes belonging to the Glu/Leu/Phe/Val dehydrogenases family. Exisiting as homohexamers, GLUD1 catalyzes the oxidative deamination of glutamate to ?ketoglutarate and ammonia while GLUD2 is involved in the recycling of glutamate during neurotransmission. GLUD1 is critical for regulating amino acid induced insulin secretion and is allosterically activated by ADP and inhibited by GTP and ATP. Mutations in the gene encoding GLUD1 causes hyperinsulinism-hyperammonemia syndrome (HHS), which is an inherited condition characterized by high insulin and ammonia levels in the blood. GLUD1 may also be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate. GLUD2 is expressed in testis and retina, with lower levels found in brain.
UOM: 1 * 100 µl
Image Unavailable-EDVO269

Experimentation kits, introduction to ELISA reactions

Catalog Number: (EDVO269)
Supplier: EDVOTEK
Description: Students learn the basic principles of the Enzyme-linked Immunosorbent Assay (ELISA) using this precise and sensitive antibody-based detection kit.
UOM: 1 * 1 items
Product Image-765-0090

Thomson e / m tube

Catalog Number: (765-0090)
Supplier: 3B Scientific
Description: Evacuated glass flask containing i.a. electron gun with directly heated tungsten wire cathode and a cylindrical, collimating anode. The generated beam is allowed to stroke along a semi-transparent mica disc in the center of the tube. Luminescent coating on the front of the disc makes the beam appear. Two of the edges of the back are provided with graduated scales.
UOM: 1 * 1 items
Image Unavailable-BOSSBS-13390R-A647

Anti-GLUD2 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-13390R-A647)
Supplier: Bioss
Description: GLUD2 is both mitochondrial matrix enzymes belonging to the Glu/Leu/Phe/Val dehydrogenases family. Exisiting as homohexamers, GLUD1 catalyzes the oxidative deamination of glutamate to ?ketoglutarate and ammonia while GLUD2 is involved in the recycling of glutamate during neurotransmission. GLUD1 is critical for regulating amino acid induced insulin secretion and is allosterically activated by ADP and inhibited by GTP and ATP. Mutations in the gene encoding GLUD1 causes hyperinsulinism-hyperammonemia syndrome (HHS), which is an inherited condition characterized by high insulin and ammonia levels in the blood. GLUD1 may also be involved in learning and memory reactions by increasing the turnover of the excitatory neurotransmitter glutamate. GLUD2 is expressed in testis and retina, with lower levels found in brain.
UOM: 1 * 100 µl
Product Image-765-1079

Demonstration thermometer

Catalog Number: (765-1079)
Supplier: MOLLER THERM
Description: Milk glass scale on polished wooden board. Colored liquid filling. Measuring range -10 to +100 ° C, 0 to +80 ° R, +20 to +212 ° F.
UOM: 1 * 1 items
Image Unavailable-BOSSBS-11272R-CY3

Anti-WFS1 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-11272R-CY3)
Supplier: Bioss
Description: Wolfram syndrome protein (WFS1) is an 890 amino acid protein that contains a cytoplasmic N-terminal domain, followed by nine-transmembrane domains and a luminal C-terminal domain. WFS1 is predominantly localized to the endoplasmic reticulum (ER) (1) and its expression is induced in response to ER stress, partially through transcriptional activation (2,3). Research studies have shown that mutations in the WFS1 gene lead to Wolfram syndrome, an autosomal recessive neurodegenerative disorder defined by young-onset, non-immune, insulin-dependent diabetes mellitus and progressive optic atrophy (4).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11272R-A350

Anti-WFS1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-11272R-A350)
Supplier: Bioss
Description: Wolfram syndrome protein (WFS1) is an 890 amino acid protein that contains a cytoplasmic N-terminal domain, followed by nine-transmembrane domains and a luminal C-terminal domain. WFS1 is predominantly localized to the endoplasmic reticulum (ER) (1) and its expression is induced in response to ER stress, partially through transcriptional activation (2,3). Research studies have shown that mutations in the WFS1 gene lead to Wolfram syndrome, an autosomal recessive neurodegenerative disorder defined by young-onset, non-immune, insulin-dependent diabetes mellitus and progressive optic atrophy (4).
UOM: 1 * 100 µl
Image Unavailable-EDVO615

ReadyPour™ Luria Broth (LB) agar base

Catalog Number: (EDVO615)
Supplier: EDVOTEK
Description: Educational Materials, Microbiology, Application: Microbiology
UOM: 1 * 1 mL
Product Image-EDVO275

Experimentation kits, simulation of HIV detection by western blot (agarose-based)

Catalog Number: (EDVO275)
Supplier: EDVOTEK
Description: The second assay used to confirm a positive HIV ELISA result is the Western blot. Using this kit, students separate protein samples from hypothetical patients on agarose gels. The proteins are then transferred to a membrane and simulated HIV proteins are detected.
UOM: 1 * 1 items
Product Image-763-0009

Kits: the case of the invisible bands, Ready-to-Load™

Catalog Number: (763-0009)
Supplier: EDVOTEK
Description: Experiment using fluorescence and electrophoresis to solve the mystery of the invisible bands.
UOM: 1 * 1 items
Image Unavailable-EDVO616

ReadyPour™ Luria Broth (LB) agar with ampicillin

Catalog Number: (EDVO616)
Supplier: EDVOTEK
Description: Educational Materials, Microbiology, Application: Microbiology, ReadyPour™ LB agar with ampicillin
UOM: 1 * 170 mL
Image Unavailable-BOSSBS-11272R

Anti-WFS1 Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-11272R)
Supplier: Bioss
Description: Wolfram syndrome protein (WFS1) is an 890 amino acid protein that contains a cytoplasmic N-terminal domain, followed by nine-transmembrane domains and a luminal C-terminal domain. WFS1 is predominantly localized to the endoplasmic reticulum (ER) (1) and its expression is induced in response to ER stress, partially through transcriptional activation (2,3). Research studies have shown that mutations in the WFS1 gene lead to Wolfram syndrome, an autosomal recessive neurodegenerative disorder defined by young-onset, non-immune, insulin-dependent diabetes mellitus and progressive optic atrophy (4).
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11272R-HRP

Anti-WFS1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-11272R-HRP)
Supplier: Bioss
Description: Wolfram syndrome protein (WFS1) is an 890 amino acid protein that contains a cytoplasmic N-terminal domain, followed by nine-transmembrane domains and a luminal C-terminal domain. WFS1 is predominantly localized to the endoplasmic reticulum (ER) (1) and its expression is induced in response to ER stress, partially through transcriptional activation (2,3). Research studies have shown that mutations in the WFS1 gene lead to Wolfram syndrome, an autosomal recessive neurodegenerative disorder defined by young-onset, non-immune, insulin-dependent diabetes mellitus and progressive optic atrophy (4).
UOM: 1 * 100 µl
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
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