6968 Results for: "1-Naphthoyl+chloride&pageNo=28"
Jacket, flame retardant, MULTISECURO
Supplier: RENTEX
Flame retardant jacket made from 55% modacrylic, 43% cotton and 2% Nega-Stat® with PTFE coating.
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Overalls / Coveralls, Overall, standard, Overalls / Coveralls, TrenkaTex®, 44 (men), Polyester/cotton, Blue, For men, 65% polyester and 35% cotton, with Sanfor®, Weight: 245 g/m², General Purpose, Pockets: With pockets, Closure type: Zip closure
Supplier: RENTEX
Overalls / Coveralls, Overall, standard, Overalls / Coveralls, TrenkaTex®, 44 (men), Polyester/cotton, Blue, For men, 65% polyester and 35% cotton, with Sanfor®, Weight: 245 g/m², General Purpose, Pockets: With pockets, Closure type: Zip closure
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Digital CO₂ measuring instrument with app connection, testo 535
Supplier: Testo
The compact CO₂ measuring instrument testo 535 with practical App connection allows you to carry out this important measurement easily and efficiently and thus ensure comfort and a healthy indoor climate. Long-term stable infrared sensor technology, the measured values are reproducible and comparable even over longer periods of time. Ideal for recurring comparative measurements. Also supported by the time and point averaging directly in the measuring instrument. By the way, the testo Smart App displays the measured values as a table or graph, stores the results and documents them. This not only makes it easy to configure the measuring instrument individually, the App also turns smartphone into a second display.
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VWR®, Accessories for Carboys, Versatile Caps, Adapters, Connectors and Spigots
Supplier: VWR Collection
VWR® has expanded the VWR® carboy features and benefits by offering the Versatile Cap, Versatile Barb and state-of-the-art Spigot technology. These three components complement a wide array of applications supported by the VWR® Carboy. The leakproof cap insert with replaceable gasket enable users to quickly change the top connector of each carboy to match the application needs. Versatile Cap is stackable and is offered in both 83 mm (compatible with most industry carboys) and a 120 mm extra wide-mouth version that fits exclusively on VWR® 20 L and 40 L extra wide mouth carboys. To see homogenisation of solutions, closed adapter inserts with a clear window are available. Quick connect options are also a part of the many capabilities of this Versatile Cap technology. This includes quick-connect port combinations of two, three, and four. For bottom tubulation, Versatile Barb is used to replace the spigot and support flexibility in drainage, connection to a pump or automated equipment, or connection to a filling bell. Sanitary fitting connector is also available in order to enable the carboy to be used as a supply reservoir to a larger system.
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Bib and braces, Overall, bib and brace, Bib and braces, TrenkaTex®, Comfort Stretch 285, 44 (men), Polyester/cotton, Blue, For men, 60% polyester, 35% cotton and 5% DOW XLA, Weight: 285 g/m², General Purpose, Industrial, Pockets: With pockets
Supplier: RENTEX
Bib and braces, Overall, bib and brace, Bib and braces, TrenkaTex®, Comfort Stretch 285, 44 (men), Polyester/cotton, Blue, For men, 60% polyester, 35% cotton and 5% DOW XLA, Weight: 285 g/m², General Purpose, Industrial, Pockets: With pockets
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QuEChERS dispersive kits
Supplier: Agilent
Step 2: Dispersive SPE cleanup
Select the dispersive SPE kit suited to the type of food being analysed and the method you are following. In this step, an aliquot of the sample extract from step one (see QuEChERS extraction kits) is added to a 2 or 15 ml centrifuge tube containing a small amount of SPE sorbent and MgSO₄. The sorbent will pull out interfering matrix materials from the sample, while the MgSO₄ helps remove excess water and improve analyte partitioning.
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Mouse Lin28A ELISA Kits
Supplier: Antibodies.com
Mouse Lin28A ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Lin28A in tissue homogenates or other biological fluids.
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Trousers, Fristads® PR54-220, Design A, royal blue
Supplier: FRISTADS KANSAS
Thanks to their durability and comfort, these trousers are perfectly suitable for use in garages as well as in industrial and service companies. The material is made of 65% polyester and 35% cotton. The inside is brushed and provides a comfortable cotton feel. The outside is very hardwearing and does not bleach, even after countless washes.
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Bib and braces, Overall, bib and brace, Bib and braces, TrenkaTex®, 50 (men), Polyester/cotton, Hi-vis yellow, For men, 60% cotton and 40% polyester, Weight: 270 g/m², HiVis, General Purpose, Industrial, Pockets: With pockets
Supplier: RENTEX
Bib and braces, Overall, bib and brace, Bib and braces, TrenkaTex®, 50 (men), Polyester/cotton, Hi-vis yellow, For men, 60% cotton and 40% polyester, Weight: 270 g/m², HiVis, General Purpose, Industrial, Pockets: With pockets
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Pilot's jacket, Icon
Supplier: FRISTADS KANSAS
Functional, two-tone winter jacket made from Beaver nylon (50% nylon, 50% cotton), a hard-wearing and tear-proof material that is resistant to dirt, oil and water. With faux fur on the collar and on the body, quilted lining in the sleeves and contrasting seams.
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Masterflex I/O Display Assembly 7575-30 Parts Assy For 7575-30 1 * 1 items
Supplier: Avantor Fluid Handling
Masterflex I/O Display Assembly 7575-30 Parts Assy For 7575-30 1 * 1 items
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Anti-C19ORF28 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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Capillary columns, TraceGOLD™ TG-5MS
Supplier: Thermo Fisher Scientific
Employ the most widely used MS phase in gas chromatography with the 5% phenyl phase Thermo Scientific TraceGOLD TG-5MS GC Column. These columns have exceptionally low bleed for optimal signal-to-noise ratio, sensitivity and MS integrity.
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High visibility jackets, 4829 PLU
Supplier: FRISTADS KANSAS
These highly visible jackets are made of 80% polyester and 20% cotton on the water-repellent outside. The other parts are made of 65% polyester and 35% cotton.
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REPLACEMENT GASKET 1 * 1 items
Supplier: Avantor Fluid Handling
REPLACEMENT GASKET 1 * 1 items
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Masterflex Polysulfone Clear Tri-Clamp Sight Gauge, 1.5'' 1 * 1 items
Supplier: Avantor Fluid Handling
Masterflex Polysulfone Clear Tri-Clamp Sight Gauge, 1.5'' 1 * 1 items
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Self-Laminating Vinyl Wrap-Around Labels for M410, BMP41, M510, BMP51, BMP53 and M511 Printers
Supplier: Brady
Mark cables and wires with the B-427 self-laminating vinyl label material, designed with a clear self-laminating protective layer. Print almost anywhere with a durable Brady portable label printer.
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Anti-C19ORF28 Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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Chemical resistant overalls, Tyvek® 600 Plus, models CHA5a / CHA6
Supplier: DuPont
These Tyvek® overalls are made from flash spun, high density polyethylene, providing an ideal balance of protection, durability and comfort. Tyvek® is permeable to both air and water vapour, yet repels water-based liquids and aerosols. It offers an excellent barrier against fine particles and fibres (down to 1 micron in size).
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Anti-C19ORF28 Rabbit Polyclonal Antibody (Cy5®)
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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Anti-C19ORF28 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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VOLCANO Multirisk Trousers
Supplier: ALSICO
Comfortable multirisk trousers in inherent flame retardant fabric.
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Anti-C19ORF28 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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Storage tubes, 2D barcoded, Matrix™
Supplier: THERMO MATRIX TECHNOLOGIES
Permanently attached, laser-etched 2D barcodes on the bottom of each tube allow you to scan and decode tubes at once without removing them from the rack and allow data to be associated with each tube.
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Anti-C19ORF28 Rabbit Polyclonal Antibody (Cy5.5®)
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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Anti-C19ORF28 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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Sharpsafe® Ecological 5th Generation Recycled Needle Containers
Supplier: Hospidex
Sharpsafe®, historic pioneer in protecting against the risk of sharps injuries and sustainability in medical waste packaging management, presents the recycled 5th generation needle containers.
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Anti-C19ORF28 Rabbit Polyclonal Antibody (Alexa Fluor® 488)
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
Expand 1 Items
Anti-C19ORF28 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
Supplier: Bioss
C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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Midnight RT PCR Expansion
Supplier: Oxford Nanopore Technologies
An expansion kit containing all the required reagents and primers to generate reverse-transcribed and PCR-amplified material from SARS-CoV-2 RNA samples.