21446 Results for: "3-Methyl-2-nitrophenyl+trifluoromethanesulphonate&pageNo=11"

Supplier: Portwest

The stylish and functional rain jacket will ensure you stand out from the crowd. Made from 300D Oxford PU coated durable stain resistant fabric, this jacket features the new Insulatex heat reflective lining panel, which reflects heat back into the body ensuring maximum warmth and comfort.

Supplier: Bioss

DNA helicase involved in cellular proliferation. Possesses DNA-dependent ATPase and helicase activities. This helicase translocates on single-stranded DNA in the 5' to 3' direction in the presence of ATP and, to a lesser extent, dATP. Its unwinding activity requires a 5'-single-stranded region for helicase loading, since flush-ended duplex structures do not support unwinding. The helicase activity is capable of displacing duplex regions up to 100 bp, which can be extended to 500 bp by RPA or the cohesion establishment factor, the Ctf18-RFC (replication factor C) complex activities. Stimulates the flap endonuclease activity of FEN1. Required for normal sister chromatid cohesion. Required for recruitement of bovine papillomavirus type 1 regulatory protein E2 to mitotic chrmosomes and for viral genome maintenance. Required for maintaining the chromosome segregation and is essential for embryonic development and the prevention of aneuploidy. May function during either S, G2, or M phase of the cell cycle. Binds to both single- and double-stranded DNA.Tissue specificity: Highly expressed in spleen, B-cells, thymus, testis, ovary, small intestine, and pancreas. Very low expression seen in the brain. Expressed in dividing cells and/or cells undergoing high levels of recombination. No expression is seen in cells signaled to terminally differentiate. Expressed in keratinocyte growth factor-stimulated cells but not in serum, EGF and IL1-beta-treated keratinocytes.

Supplier: Bioss

DNA helicase involved in cellular proliferation. Possesses DNA-dependent ATPase and helicase activities. This helicase translocates on single-stranded DNA in the 5' to 3' direction in the presence of ATP and, to a lesser extent, dATP. Its unwinding activity requires a 5'-single-stranded region for helicase loading, since flush-ended duplex structures do not support unwinding. The helicase activity is capable of displacing duplex regions up to 100 bp, which can be extended to 500 bp by RPA or the cohesion establishment factor, the Ctf18-RFC (replication factor C) complex activities. Stimulates the flap endonuclease activity of FEN1. Required for normal sister chromatid cohesion. Required for recruitement of bovine papillomavirus type 1 regulatory protein E2 to mitotic chrmosomes and for viral genome maintenance. Required for maintaining the chromosome segregation and is essential for embryonic development and the prevention of aneuploidy. May function during either S, G2, or M phase of the cell cycle. Binds to both single- and double-stranded DNA.Tissue specificity: Highly expressed in spleen, B-cells, thymus, testis, ovary, small intestine, and pancreas. Very low expression seen in the brain. Expressed in dividing cells and/or cells undergoing high levels of recombination. No expression is seen in cells signaled to terminally differentiate. Expressed in keratinocyte growth factor-stimulated cells but not in serum, EGF and IL1-beta-treated keratinocytes.

Supplier: Bioss

DNA helicase involved in cellular proliferation. Possesses DNA-dependent ATPase and helicase activities. This helicase translocates on single-stranded DNA in the 5' to 3' direction in the presence of ATP and, to a lesser extent, dATP. Its unwinding activity requires a 5'-single-stranded region for helicase loading, since flush-ended duplex structures do not support unwinding. The helicase activity is capable of displacing duplex regions up to 100 bp, which can be extended to 500 bp by RPA or the cohesion establishment factor, the Ctf18-RFC (replication factor C) complex activities. Stimulates the flap endonuclease activity of FEN1. Required for normal sister chromatid cohesion. Required for recruitement of bovine papillomavirus type 1 regulatory protein E2 to mitotic chrmosomes and for viral genome maintenance. Required for maintaining the chromosome segregation and is essential for embryonic development and the prevention of aneuploidy. May function during either S, G2, or M phase of the cell cycle. Binds to both single- and double-stranded DNA.Tissue specificity: Highly expressed in spleen, B-cells, thymus, testis, ovary, small intestine, and pancreas. Very low expression seen in the brain. Expressed in dividing cells and/or cells undergoing high levels of recombination. No expression is seen in cells signaled to terminally differentiate. Expressed in keratinocyte growth factor-stimulated cells but not in serum, EGF and IL1-beta-treated keratinocytes.

Supplier: CONTEC

QuickTask™ mopping system. The QuickTask™ product line consists of a variety of knitted polyester, polyester/cellulose, microfibre/foam and microfibre flat mop heads that are easily installed onto a hinged mop head frame and QuickConnect interchangeable handle. QuickTask™ mop head frames are available in stainless steel or durable, autoclavable polypropylene.

Supplier: Cayman Chemical

11β-13,14-dihydro-15-keto Prostaglandin F2α-d4 1 * 50 µG

Supplier: Thermo Fisher Scientific

TIP CONE MODULE 1-CH.40-200UL 1 * 1 items

Supplier: GETINGE LIFE SCIENCES

PANEL CONTROL 1 * 1 items

Supplier: NEUBERT VOLUME GLASSWAERE

CRUCIBLE LOW FORM 11ML NO LID QUARTZ 1 * 1 items

Supplier: Cayman Chemical

2,3-DINOR-11Β-PROSTAGLANDIN F2Α-D9 1 * 50 µG

Supplier: GETINGE LIFE SCIENCES

RUNNER WHEEL 1 * 1 items

Supplier: EPPENDORF

ROTOR COVER 1 * 1 items

Supplier: Greisinger

CASE GKK252 PLASTIC 235X185X48MM 1 * 1 items

Supplier: MACHEREY-NAGEL

Filter paper folded MN 704 1/4 11cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper folded MN 611 1/4 11cm diameter, pack of 100. 1 * 100 items

Supplier: Merck

Monolithic silica technology: A new age in chromatography. Chromolith® columns are based on silica so existing methods can be easily transferred with only minimal investment in new method development work. 'Sol-Gel' technology allows highly porous monolithic rods of silica to be formed. These feature a bimodal pore structure provides a unique combination of macropores and mesopores.

Supplier: GETINGE LIFE SCIENCES

SPRING DOOR CATCH 1 * 1 items

Supplier: SCHURR SCHUHVERTRIEB

SANDAL HAMBURG WHITE SIZE 40 1 * 1 PAIR

Supplier: SCHURR SCHUHVERTRIEB

SANDAL HAMBURG WHITE SIZE 46 1 * 1 PAIR

Supplier: SCHURR SCHUHVERTRIEB

SANDAL HAMBURG WHITE SIZE 41 1 * 1 PAIR

Supplier: GETINGE LIFE SCIENCES

SPRING COLUMN NON RETURN VALVE 1 * 1 items

Supplier: UVEX

Leather Glove HexArmor Chrome Series 4080 size XXL 1 * 1 PAIR

Supplier: LGC Standards PROMOCHEM

Aqueous Ethanol Standard (0.5 g/l) 10 x 1.2 mL 1 * 10 items

Supplier: SCHURR SCHUHVERTRIEB

SANDAL HAMBURG WHITE SIZE 43 1 * 1 PAIR

Supplier: DELTA T

ICE ACCU S 170ML 1 * 1 items

Supplier: SCHURR SCHUHVERTRIEB

SANDAL HAMBURG WHITE SIZE 38 1 * 1 PAIR

Supplier: SCHURR SCHUHVERTRIEB

SANDAL HAMBURG WHITE SIZE 45 1 * 1 PAIR

Supplier: SCHURR SCHUHVERTRIEB

SANDAL HAMBURG WHITE SIZE 42 1 * 1 PAIR

Supplier: Portwest

This superb 5-in-1 jacket system is adaptable for any work situation. Outer jacket features 2 large roomy pockets, stud adjustable cuffs and concealed attached roll-away hood. Inner jacket has fluorescent fleece sleeves, comfortable knitted cuffs and 2 side pockets. Both the inner and outer jacket have full EN ISO 20471 Class 3 certification for maximum high visibility protection and safety.

Supplier: BIOPREMIER

Food safe kits provide a simple, reliable, and rapid procedure for detecting the presence of a specific pathogenic bacteria. The assay is based on 5’ nuclease Real-Time PCR reactions to amplify a unique genomic sequence in the target microorganism. PCR is a method used to amplify a specific DNA sequence which is typically amplified in a reaction containing a thermostable DNA polymerase, nucleotides, and primers complementary to the target sequence. When this solution is heated, the DNA molecule denatures, separating into two strands. As the solution cools, the primers anneal to the target sequences in the separated DNA strands and the DNA polymerase synthesises a new strand by extending the primers with nucleotides, creating a copy of the DNA sequence (amplicons). When repeated, this cycle of denaturing, annealing, and extending exponentially increases the number of target amplicons. In Real-Time PCR, specific fluorescent probes are used to detect the amplified DNA by hybridising with amplicons. These probes are linked to a fluorophore on one end and a quencher that suppresses fluorescence on the other. If the target sequence is present during the PCR, amplification occurs and the probe is degraded, resulting in fluorescence increase. Fluorescence is measured by a detector and the associated software plots the fluorescence intensity versus number of cycles, allowing the determination of the presence or absence of the target organism.