15973 Results for: "Amberlite\u00AE+IRA-67&pageNo=24&view=list"

Supplier: MACHEREY-NAGEL

Filter paper circles MN 875 24cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 651 24cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 621 24cm diameter, pack of 100. 1 * 100 items

Supplier: Thermo Scientific

HANDLE D=24MM H=22MM FOR GLASS DOOR 1 * 1 items

Supplier: Thermo Scientific

Iq/oq plate shuttle system up to 24pc d 1 * 1 items

Supplier: SciLabware

Flask volumetric pyrex, class A, amber coloured, 1000 ml, ukas certified 1 * 1 items

Supplier: witeg Labortechnik

Flask Erlenmeyer, 150ml, ST24/29, borosilicate glass 3.3 1 * 1 items

Supplier: CONNECTICUT CLEANROOM

MAT FRAME SHEET ALU 24X42IN 1 * 1 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 704 24cm diameter, pack of 100. 1 * 100 items

Supplier: MARIENFELD

COLOR PLATE WITH 12 DEPRESSIONS 1 * 1 items

Supplier: Hach

TUBES SPECIMEN MPN 24ML 1 * 10 items

Supplier: Brand

PP. Eight connected 0,2 ml tubes and domed or flat caps in strips of eight.

Supplier: MACHEREY-NAGEL

Filter paper circles MN 605 24cm diameter, pack of 100. 1 * 100 items

Supplier: MACHEREY-NAGEL

Filter paper circles MN 652 24cm diameter, pack of 100. 1 * 100 items

Supplier: Industrial Physics

BK-6 drying recorder 240v/50hz 1 * 1 items

Supplier: G-Biosciences

Determination of protein concentration is an essential technique in all aspects of protein studies and proteomics. The Assays for Protein Quantification kit includes three of the most widely used protein assays and allows for a direct comparison of the three assays that teaches students the benefits and limitations of each assay. Each assay is available individually to allow teaching of a specific assay, without the option of comparing and contrasting with other assays. The three assays covered are the Biuret Protein Assay, Lowry Protein Assay and the Coomassie Blue Dye Protein Assay. The Assays for Protein Quantification kit provides all the reagents required to perform both protein assays, including protein standards for accurate quantification, in a single lab activity. An often underestimated factor in quantifying protein is the presence of non-protein interfering agents, such as salts and detergents. This kit teaches students about common laboratory agents that affect the protein assays, the reasoning behind their interferences and how to overcome the interference. Students also learn how to select a protein assay for different applications.

Supplier: ProSci Inc.

FBXO24 is a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein belongs to the Fbxs class. Alternative splicing of this gene generates two transcript variants. This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class. Alternative splicing of this gene generates two transcript variants.

Supplier: DELTA T

COOLING BRICK 22C 600ML / 190X121X34 1 * 1 items

Supplier: Industrial Physics

BK-3 Drying Recorder 240v/50hz 1 * 1 items

Supplier: SHP Steriltechnik

Printer switch mode power supply 12W 5V/ 2, A 1 * 1 items

Supplier: Thermo Scientific

2/2-way solenoid valve G1/4, Y2, 6.5B, 1 * 1 items

Supplier: Greiner Bio-One

SENSOPLATE 24W GLASS BOTTOM W/O LID ST 1 * 12 items

Supplier: KNF CLEANROOM

BAGS PE 2MIL ANTISTATIC PINK24”X36”X.002 1 * 1.000 items

Supplier: Thermo Scientific

Iq/oq plate shuttle system up to 24pc gb 1 * 1 items

Supplier: Basan

MOPHEAD TRAPEZE SPARK 40X10 CM 1 * 1 items

Supplier: CONNECTICUT CLEANROOM

FRAME MAT SHEET ALU 30 X 42 IN 1 * 1 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: 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: Brand

PP. Eight connected 0,2 ml tubes with attached domed cap strips.