Wyszukano: HAEP+LABOR

Producent: Merck

Opis: Aldehyd izowalerianowy, Sigma-Aldrich®

Producent: Merck

Opis: Aldehyd izowalerianowy, Sigma-Aldrich®

Numer katalogowy: (PRSI56-299)

Producent: ProSci Inc.

Opis: This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols using NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme binds bile acid with high affinity, and shows minimal 3-alpha-hydroxysteroid dehydrogenase activity. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14.

j.m.: 1 * 400 µl

New Product Wyprzedaż

Producent: Merck

Opis: aldehyd 4-hydroksybenzylowy, Sigma-Aldrich®

Producent: Merck

Opis: Aldehyd maslowy, Sigma-Aldrich®

Numer katalogowy: (SIAL434086-5G)

Producent: Merck

Opis: 2-Hydroxy-3-methoxy-5-nitrobenzaldehyde, Sigma-Aldrich®

j.m.: 1 * 5 g

Wyprzedaż

Numer katalogowy: (442719.)

Producent: Merck

Opis: Pelargonaldehyd analytical standard, Supelco®

j.m.: 1 * 1 SZT

Wyprzedaż

Producent: Merck

Opis: Aldehyd maslowy do syntezy, Sigma-Aldrich®

Producent: UVEX

Opis: Te nie wzmacniane rękawice wykonane w 100% z kauczuku butylowego zapewniają dobrą odporność na związki polarne, takie jak estry, ketony, aldehydy, aminy i nasycone roztwory soli, a także kwasy i zasady.

Producent: MP Biomedicals

Opis: A modified tripeptide reversible protease inhibitor of trypsin-like proteases and some cysteine proteases including endoproteinase Lys-C, kallikrein, papain, thrombin, cathepsin B, cathepsins H and L, trypsin, calpain, trypsin and plasmin. Little to no inhibition is seen against pepsin, cathepsins A and D and alpha-chymotrypsin. When adjusted for molarity, all three salt forms are equally effective; however, the hydrochloride salt is usually less invasive in biological settings. Leupeptin, because of its aldehyde group, may act as a reducing agent and therefore interfere in protein determinations such as Lowry and, to a lesser extent, Bradford.

Producent: POCH AVANTOR BRAND

Opis: 4-dimetyloaminobenzaldehyd, czysty reagent analityczny

Producent: Merck

Opis: aldehyd 4-hydroksybenzylowy, Sigma-Aldrich®

Producent: Merck

Opis: aldehyd 4-hydroksybenzylowy for synthesis, Sigma-Aldrich®

MSDS

Producent: Merck

Opis: The Aquastar® range is designed to provide reagents for the determination of water by Karl Fischer titration of a wide range of substrates and by a variety of methodologies. These include reagents for one- or two-component systems; combined coulometric reagents; solvents for oils and fats; reagents and solvents for determination of water in ketones and aldehydes. Calibration standards are also available.

Producent: G-Biosciences

Opis: HOOK™ Biotin-Hydrazide and its long spacer arm equivalent, HOOK™ Biotin-LC-Hydrazide, are carbohydrate reactive reagents. HOOK™ carbohydrate reactive biotin reagents react with oxidised carbohydrate side chains. Some biotin reagents do not bind directly to the protein itself, but instead, conjugate to the carbohydrate residues of glycoproteins. The carbohydrate reactive biotin reagents contain hydrazides (-NH-NH₂) as a reactive group. The hydrazide reactions require carbonyl groups, such as aldehydes and ketones, which are formed by oxidative treatment of the carbohydrates. Hydrazides react spontaneously with carbonyl groups, forming a stable hydrazone bond. These reagents are particularly suitable for labelling and studying glycosylated proteins, such as antibodies and receptors.

Numer katalogowy: (PRSI91-710)

Producent: ProSci Inc.

Opis: AKR1C3, is an enzyme which belongs to the aldo/keto reductase family. It is expressed in many tissues including adrenal gland, brain, kidney, liver, lung, mammary gland, placenta, small intestine, colon, spleen, prostate and testis. AKR1C3 catalyses the conversion of aldehydes and ketones to alcohols. It catalyses the reduction of prostaglandin (PG) D2, PGH2 and phenanthrenequinone (PQ) and the oxidation of 9-alpha,11-beta-PGF2 to PGD2,which functions as a bi-directional 3-alpha-, 17-beta- and 20-alpha HSD. It can interconvert active androgens, estrogens and progestins with their cognate inactive metabolites.

j.m.: 1 * 50 µG

Wyprzedaż