15163 Results for: "Tetramethylammonium+hydrogen+sulphate&pageNo=24"

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIGPPNEONORANGE 1 * 1 items

Supplier: MP Biomedicals

FastRNA® Pro Blue Kit is used to isolate total RNA from gram positive and gram negative bacteria. Isolated RNA is suitable for RT-PCR analysis and other downstream applications.

Supplier: Sartorius

FILTER FOLDED ANALYTICAL FAST SPONGY DIAMETER-240MM 1 * 100 items

Supplier: Bioss

Multiubiquitin chain receptor involved in modulation of proteasomal degradation. Binds to polyubiquitin chains. Proposed to be capable to bind simultaneously to the 26S proteasome and to polyubiquitinated substrates and to deliver ubiquitinated proteins to the proteasome. May play a role in endoplasmic reticulum-associated degradation (ERAD) of misfolded glycoproteins by association with PNGase and delivering deglycosylated proteins to the proteasome. Involved in global genome nucleotide excision repair (GG-NER) by acting as component of the XPC complex. Cooperatively with CETN2 appears to stabilise XPC. May protect XPC from proteasomal degradation. The XPC complex is proposed to represent the first factor bound at the sites of DNA damage and together with other core recognition factors, XPA, RPA and the TFIIH complex, is part of the pre-incision (or initial recognition) complex. The XPC complex recognises a wide spectrum of damaged DNA characterised by distortions of the DNA helix such as single-stranded loops, mismatched bubbles or single-stranded overhangs. The orientation of XPC complex binding appears to be crucial for inducing a productive NER. XPC complex is proposed to recognise and to interact with unpaired bases on the undamaged DNA strand which is followed by recruitment of the TFIIH complex and subsequent scanning for lesions in the opposite strand in a 5'-to-3' direction by the NER machinery. Cyclobutane pyrimidine dimers (CPDs) which are formed upon UV-induced DNA damage esacpe detection by the XPC complex due to a low degree of structural perurbation. Instead they are detected by the UV-DDB complex which in turn recruits and cooperates with the XPC complex in the respective DNA repair. In vitro, the XPC:RAD23B dimer is sufficient to initiate NER; it preferentially binds to cisplatin and UV-damaged double-stranded DNA and also binds to a variety of chemically and structurally diverse DNA adducts.

Supplier: Bioss

Multiubiquitin chain receptor involved in modulation of proteasomal degradation. Binds to polyubiquitin chains. Proposed to be capable to bind simultaneously to the 26S proteasome and to polyubiquitinated substrates and to deliver ubiquitinated proteins to the proteasome. May play a role in endoplasmic reticulum-associated degradation (ERAD) of misfolded glycoproteins by association with PNGase and delivering deglycosylated proteins to the proteasome. Involved in global genome nucleotide excision repair (GG-NER) by acting as component of the XPC complex. Cooperatively with CETN2 appears to stabilise XPC. May protect XPC from proteasomal degradation. The XPC complex is proposed to represent the first factor bound at the sites of DNA damage and together with other core recognition factors, XPA, RPA and the TFIIH complex, is part of the pre-incision (or initial recognition) complex. The XPC complex recognises a wide spectrum of damaged DNA characterised by distortions of the DNA helix such as single-stranded loops, mismatched bubbles or single-stranded overhangs. The orientation of XPC complex binding appears to be crucial for inducing a productive NER. XPC complex is proposed to recognise and to interact with unpaired bases on the undamaged DNA strand which is followed by recruitment of the TFIIH complex and subsequent scanning for lesions in the opposite strand in a 5'-to-3' direction by the NER machinery. Cyclobutane pyrimidine dimers (CPDs) which are formed upon UV-induced DNA damage esacpe detection by the XPC complex due to a low degree of structural perurbation. Instead they are detected by the UV-DDB complex which in turn recruits and cooperates with the XPC complex in the respective DNA repair. In vitro, the XPC:RAD23B dimer is sufficient to initiate NER; it preferentially binds to cisplatin and UV-damaged double-stranded DNA and also binds to a variety of chemically and structurally diverse DNA adducts.

Supplier: BEHR

HEATING KIT 2000W FOR SMA24/HAT 1 * 1 items

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIG PP BLUE 1 * 1 items

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIG PP RED 1 * 1 items

Supplier: USA SCIENTIFIC PLASTICS

RACK FLIPPER- 4-SEITIG PP ORANGE 1 * 1 items

Supplier: CUSTOM MADE CHEMICALS LAB

53 components mix 1 * 2 Ampoul

Supplier: KOEHLER TECHNISCHE PRODUKTEN

Rack, flipper 1, colour green, material PP, autoclavable, temperature resistant -90C to +120C, dimension 197x95x115mm, 8 holes dia meter 30mm, 20 holes diameter 20mm. 1 * 1 items

Supplier: KOEHLER TECHNISCHE PRODUKTEN

Rack, flipper 1, colour blue, material PP, autoclavable, temperature resistant -90C to +120C, dimension 197x95x115mm, 8 holes diam eter 30mm, 20 holes diameter 20mm. 1 * 1 items

Supplier: OMEGA BIO-TEK

Pre-scripted solution for the purification of cfDNA from up to 4 ml plasma samples.

Supplier: KOEHLER TECHNISCHE PRODUKTEN

Rack, flipper 1, colour yellow, material PP, autoclavable, temperature resistant -90C to +120C, dimension 197x95x115mm, 8 holes di ameter 30mm, 20 holes diameter 20mm. 1 * 1 items

Supplier: KOEHLER TECHNISCHE PRODUKTEN

Rack, flipper 1, colour orange, material PP, autoclavable, temperature resistant -90C to +120C, dimension 197x95x115mm, 8 holes di ameter 30mm, 20 holes diameter 20mm. 1 * 1 items

Supplier: HONEYWELL SAFETY

GLOVE DEXPURE 803-81 NITRILE PF XL 1 * 200 items

Supplier: CUSTOM MADE CHEMICALS LAB

36 COMPONENTS MIX 1 * 2 items

Supplier: DWK Life Sciences

Centrifuge Tube, Screw Thread,50ml, conical shaped bottom 1 * 12 items

Supplier: SIGMUND LINDNER

LINDNER SILIBEADS TYP S 2.00-2.40 MM 1 * 1 kg

Supplier: BELLCO GLASS

AUTOCLAVE STERILIZATION BAG 12 X 24INCH 1 * 100 items

Supplier: OMEGA BIO-TEK

The Mag-Bind® cfDNA Kit is designed for rapid and reliable isolation of circulating DNA from 500 to 4000 µl plasma or serum samples. The Mag-Bind® cfDNA Kit can be processed manually or with automated platforms. The procedure eliminates the need for funnels and vacuum steps, providing hands-free operation in automated protocols.

Supplier: Bioss

Multiubiquitin chain receptor involved in modulation of proteasomal degradation. Binds to polyubiquitin chains. Proposed to be capable to bind simultaneously to the 26S proteasome and to polyubiquitinated substrates and to deliver ubiquitinated proteins to the proteasome. May play a role in endoplasmic reticulum-associated degradation (ERAD) of misfolded glycoproteins by association with PNGase and delivering deglycosylated proteins to the proteasome. Involved in global genome nucleotide excision repair (GG-NER) by acting as component of the XPC complex. Cooperatively with CETN2 appears to stabilise XPC. May protect XPC from proteasomal degradation. The XPC complex is proposed to represent the first factor bound at the sites of DNA damage and together with other core recognition factors, XPA, RPA and the TFIIH complex, is part of the pre-incision (or initial recognition) complex. The XPC complex recognises a wide spectrum of damaged DNA characterised by distortions of the DNA helix such as single-stranded loops, mismatched bubbles or single-stranded overhangs. The orientation of XPC complex binding appears to be crucial for inducing a productive NER. XPC complex is proposed to recognise and to interact with unpaired bases on the undamaged DNA strand which is followed by recruitment of the TFIIH complex and subsequent scanning for lesions in the opposite strand in a 5'-to-3' direction by the NER machinery. Cyclobutane pyrimidine dimers (CPDs) which are formed upon UV-induced DNA damage esacpe detection by the XPC complex due to a low degree of structural perurbation. Instead they are detected by the UV-DDB complex which in turn recruits and cooperates with the XPC complex in the respective DNA repair. In vitro, the XPC:RAD23B dimer is sufficient to initiate NER; it preferentially binds to cisplatin and UV-damaged double-stranded DNA and also binds to a variety of chemically and structurally diverse DNA adducts.

Supplier: Bioss

Multiubiquitin chain receptor involved in modulation of proteasomal degradation. Binds to polyubiquitin chains. Proposed to be capable to bind simultaneously to the 26S proteasome and to polyubiquitinated substrates and to deliver ubiquitinated proteins to the proteasome. May play a role in endoplasmic reticulum-associated degradation (ERAD) of misfolded glycoproteins by association with PNGase and delivering deglycosylated proteins to the proteasome. Involved in global genome nucleotide excision repair (GG-NER) by acting as component of the XPC complex. Cooperatively with CETN2 appears to stabilise XPC. May protect XPC from proteasomal degradation. The XPC complex is proposed to represent the first factor bound at the sites of DNA damage and together with other core recognition factors, XPA, RPA and the TFIIH complex, is part of the pre-incision (or initial recognition) complex. The XPC complex recognises a wide spectrum of damaged DNA characterised by distortions of the DNA helix such as single-stranded loops, mismatched bubbles or single-stranded overhangs. The orientation of XPC complex binding appears to be crucial for inducing a productive NER. XPC complex is proposed to recognise and to interact with unpaired bases on the undamaged DNA strand which is followed by recruitment of the TFIIH complex and subsequent scanning for lesions in the opposite strand in a 5'-to-3' direction by the NER machinery. Cyclobutane pyrimidine dimers (CPDs) which are formed upon UV-induced DNA damage esacpe detection by the XPC complex due to a low degree of structural perurbation. Instead they are detected by the UV-DDB complex which in turn recruits and cooperates with the XPC complex in the respective DNA repair. In vitro, the XPC:RAD23B dimer is sufficient to initiate NER; it preferentially binds to cisplatin and UV-damaged double-stranded DNA and also binds to a variety of chemically and structurally diverse DNA adducts.

Supplier: Sartorius

FILTER DISC CELLULOSE PAPER MODERATELY FAST DIAMETER-240MM 1 * 100 items

Supplier: MARKET SOURCE PART PROCESS

CELL BAC-OPTIMIZED REPLICATOR V2.0 ELECTROCOMPETENT CELLS, 1 * 1 items

Supplier: LIEDER JOHANNES

Mitosis and Meiosis. Atlas of 25 OHP Transparencies size 22 x 28 cm, comprising over 95 color pictures. Specially selected and beaut iful multicolored photomicrographs are presented on this atlas together with explaing drawings, diagrams and tables. 1 * 25 items

Supplier: Brand

PP. Eight connected 0,2 or 0,15 ml PCR tubes with attached flat individual caps. The tubes are held together by three connectors for increased rigidity.

Supplier: MACHEREY-NAGEL

Filter paper circles MN 640 mf 24cm diameter, pack of 100. 1 * 100 items

Supplier: Genscript

The AmMag Quatro is an automated solution for purification of large-scale, high quality, transfection-grade plasmids from Escherichia coli cultures.

Supplier: Heidolph Instruments GmbH & Co.KG

Models PD 5201 and PD 5206 for advanced requirements. Peristaltic pumps are ideal for transporting and metering aggressive, abrasive, or corrosive solutions, and also for sterile media under low pressure. The medium to be transported only comes into contact with the tubing, so there is no contamination. Suitable for transporting highly viscous media up to 10000 mPas. The pumps are self-priming without seals or valves. Can be used in the food industry for filtering and separating, for water treatment, in biotechnology and routine laboratory applications. Media can be transported under pressure and under vacuum. Maintenance-free motors ensure long service life. Quantities displaced by the pump heads are stored in the program depending on the individual tubes used, and are shown in the digital display. Software may be ordered separately as an accessory. The pump drive is microprocessor-controlled. Equipped with RS232 digital interface; speed, metered quantity, flow rate, pause, and tube dimension can be controlled. Digital display of speed (min⁻¹) and flow rate (ml/min). Digital display of displacement volume (ml) in the case of volume metering. Intermittent metering is available with adjustable pause times. A metered volume can also be specified in addition to the flow rate display. Extremely simple calibration of displacement volume (ml) and flow rate (ml/min).