Hledali jste: Sl\u00E1mky+kryogenn\u00ED

Katalogové číslo: (MSGA30606005)

Dodavatel: asecos

Popis: [EN]CABINET SAFETY STORAGE SL.196.120.MV 1 * 1 KS

Měrná jednotka: 1 * 1 KS

Akce

Katalogové číslo: (ERLANR2201KK09)

Dodavatel: ERLAB CAPTAIRE

Popis: [EN]FILTER CARB KK FOR SCHOOL UNIT SL/S 1 * 1 KS

Měrná jednotka: 1 * 1 KS

Akce

Katalogové číslo: (SORV76806)

Dodavatel: Thermo Fisher Scientific

Popis: [EN]ADAPTER RTR MACH SL-250T ST-H5 1 * 1 KS

Měrná jednotka: 1 * 1 KS

Akce

Katalogové číslo: (ABCAAB249862-100)

Dodavatel: Abcam

Popis: [EN][EN]RABBIT MONOCLONAL EPR11581 TO SL 1 * 100 µG

Měrná jednotka: 1 * 100 µG

Akce

Katalogové číslo: (MSGA30613001)

Dodavatel: asecos

Popis: Skříň křídlové dveře 600x605x1970mm, pravý závěs dveří, korpus/dveře RAL 7035/RAL 7035 (světle šedá/světle šedá), mod el line SL-LIN E, model group SL-CLASSIC, model SL.196.060.MH 1 * 1 KS

Měrná jednotka: 1 * 1 KS

Akce

Katalogové číslo: (BRDY312029)

Dodavatel: Brady

Popis: [EN]LABEL BM-06-7593-SL 500/ROLL 1 * 1 Roll

Měrná jednotka: 1 * 1 Roll

Akce

Katalogové číslo: (BSBTFEK0504)

Dodavatel: Boster Bio

Popis: MOUSE SL-SELECTIN FAST ELISA KIT 96 WELL 1 * 1 KIT

Měrná jednotka: 1 * 1 KIT

Akce

Katalogové číslo: (BSBTFEK0503)

Dodavatel: Boster Bio

Popis: HUMAN SL-SELECTIN FAST ELISA KIT 96 WELL 1 * 1 KIT

Měrná jednotka: 1 * 1 KIT

Akce

Katalogové číslo: (SCOR1033805)

Dodavatel: Schott AG

Popis: [EN]ROD CONTURAX CD041 299S L-1500 SL-29 1 * 12 kg

Měrná jednotka: 1 * 12 kg

Akce

Katalogové číslo: (JULA7.901.1065)

Dodavatel: JULABO GmbH

Popis: [EN]PUMP SET 50-60HZ (HE, HL, SE, SL, HL 1 * 1 KS

Měrná jednotka: 1 * 1 KS

Akce

Katalogové číslo: (BOSSBS-11797R-A555)

Dodavatel: Bioss

Popis: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-11797R-A680)

Dodavatel: Bioss

Popis: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyses the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterised by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-11797R-CY7)

Dodavatel: Bioss

Popis: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-11797R-FITC)

Dodavatel: Bioss

Popis: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-11797R-CY3)

Dodavatel: Bioss

Popis: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

Měrná jednotka: 1 * 100 µl

Akce

Katalogové číslo: (BOSSBS-11797R-HRP)

Dodavatel: Bioss

Popis: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

Měrná jednotka: 1 * 100 µl

Akce