U heeft gezocht op: Basismaterialen+voor+microbiologie

Omschrijving: [EN]VOL.FLASK 100ML NS12/21 A HOLLOW GLA 1 * 2 ST

Catalogus nummer: HIRS2820280

UOM: 1 * 2 ST

Leverancier: HIRSCHMANN

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Omschrijving: [EN]VOL.FLASK 500ML NS19/26 A HOLLOW GLA 1 * 2 ST

Catalogus nummer: HIRS2820290

UOM: 1 * 2 ST

Leverancier: HIRSCHMANN

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Omschrijving: [EN]VOL.FLASK 20ML NS10/19 A HOLLOW GLAS 1 * 2 ST

Catalogus nummer: HIRS2820265

UOM: 1 * 2 ST

Leverancier: HIRSCHMANN

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Omschrijving: VOL.FLASK 25ML NS12/21 A HOLLOW GLAS WI 1 * 2 ST

Catalogus nummer: HIRS2820271

UOM: 1 * 2 ST

Leverancier: HIRSCHMANN

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Omschrijving: [EN]VOL.FLASK 200ML NS14/23 A HOLLOW GLA 1 * 2 ST

Catalogus nummer: HIRS2820285

UOM: 1 * 2 ST

Leverancier: HIRSCHMANN

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Omschrijving: Chromium potassium sulfate is the potassium double sulfate of chromium.

Catalogus nummer: ICNA0219403190

UOM: 1 * 500 g

Leverancier: MP Biomedicals

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Omschrijving: RFESD, also known as Rieske domain-containing protein, is a 157 amino acid protein that binds one 2Fe-2S cluster per subunit. Involved in metal ion binding, RFESD contains one Rieske domain. The RFESD gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 5q15. Chromosome 5 makes up approximately 6% of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Catalogus nummer: BOSSBS-8496R-HRP

UOM: 1 * 100 µl

Leverancier: Bioss

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Omschrijving: Located in the mitochondrial inner membrane, mitochondrial complex I is the first and largest enzyme in the electron transport chain of oxidative phosphorylation. By oxidizing NADH that is produced in the Krebs cycle, this complex utilizes the two electrons to reduce ubiquinone to ubiquinol, thereby initiating the passage of electrons to successive complexes and ultimately leading to the reduction of oxygen to water. Mitochondrial complex I consists of over 40 subunits and is of considerable clinical interest since defects in any of the subunits can lead to various myopathies and neuropathies. As a subunit of mitochondrial complex I, NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7), also designated NADH-ubiquinone oxidoreductase 20 kDa subunit, is a 213 amino acid protein that is suggested to be required for catalytic activity. Defects in the gene encoding NDUFS7 are the cause of Leigh syndrome, a severe neurological disorder that is characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.

Catalogus nummer: BOSSBS-11734R-HRP

UOM: 1 * 100 µl

Leverancier: Bioss

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Omschrijving: Located in the mitochondrial inner membrane, mitochondrial complex I is the first and largest enzyme in the electron transport chain of oxidative phosphorylation. By oxidizing NADH that is produced in the Krebs cycle, this complex utilizes the two electrons to reduce ubiquinone to ubiquinol, thereby initiating the passage of electrons to successive complexes and ultimately leading to the reduction of oxygen to water. Mitochondrial complex I consists of over 40 subunits and is of considerable clinical interest since defects in any of the subunits can lead to various myopathies and neuropathies. As a subunit of mitochondrial complex I, NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7), also designated NADH-ubiquinone oxidoreductase 20 kDa subunit, is a 213 amino acid protein that is suggested to be required for catalytic activity. Defects in the gene encoding NDUFS7 are the cause of Leigh syndrome, a severe neurological disorder that is characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.

Catalogus nummer: BOSSBS-11734R-A350

UOM: 1 * 100 µl

Leverancier: Bioss

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Omschrijving: [EN]TRACE METALS IN DRINKING WATER STAND 1 * 100 mL

Catalogus nummer: ACSDA19C2N01F.L1

UOM: 1 * 100 mL

Leverancier: CPACHEM

New Product Sale

Omschrijving: [EN]BOTTLE CALIB. MIX 125ML 500 PPM MAJO 1 * 1 ST

Catalogus nummer: VARI6610030700

UOM: 1 * 1 ST

Leverancier: VARIAN

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Omschrijving: Located in the mitochondrial inner membrane, mitochondrial complex I is the first and largest enzyme in the electron transport chain of oxidative phosphorylation. By oxidizing NADH that is produced in the Krebs cycle, this complex utilizes the two electrons to reduce ubiquinone to ubiquinol, thereby initiating the passage of electrons to successive complexes and ultimately leading to the reduction of oxygen to water. Mitochondrial complex I consists of over 40 subunits and is of considerable clinical interest since defects in any of the subunits can lead to various myopathies and neuropathies. As a subunit of mitochondrial complex I, NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7), also designated NADH-ubiquinone oxidoreductase 20 kDa subunit, is a 213 amino acid protein that is suggested to be required for catalytic activity. Defects in the gene encoding NDUFS7 are the cause of Leigh syndrome, a severe neurological disorder that is characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.

Catalogus nummer: BOSSBS-11734R-FITC

UOM: 1 * 100 µl

Leverancier: Bioss

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Omschrijving: Located in the mitochondrial inner membrane, mitochondrial complex I is the first and largest enzyme in the electron transport chain of oxidative phosphorylation. By oxidizing NADH that is produced in the Krebs cycle, this complex utilizes the two electrons to reduce ubiquinone to ubiquinol, thereby initiating the passage of electrons to successive complexes and ultimately leading to the reduction of oxygen to water. Mitochondrial complex I consists of over 40 subunits and is of considerable clinical interest since defects in any of the subunits can lead to various myopathies and neuropathies. As a subunit of mitochondrial complex I, NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7), also designated NADH-ubiquinone oxidoreductase 20 kDa subunit, is a 213 amino acid protein that is suggested to be required for catalytic activity. Defects in the gene encoding NDUFS7 are the cause of Leigh syndrome, a severe neurological disorder that is characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.

Catalogus nummer: BOSSBS-11734R-A488

UOM: 1 * 100 µl

Leverancier: Bioss

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Omschrijving: Located in the mitochondrial inner membrane, mitochondrial complex I is the first and largest enzyme in the electron transport chain of oxidative phosphorylation. By oxidizing NADH that is produced in the Krebs cycle, this complex utilizes the two electrons to reduce ubiquinone to ubiquinol, thereby initiating the passage of electrons to successive complexes and ultimately leading to the reduction of oxygen to water. Mitochondrial complex I consists of over 40 subunits and is of considerable clinical interest since defects in any of the subunits can lead to various myopathies and neuropathies. As a subunit of mitochondrial complex I, NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7), also designated NADH-ubiquinone oxidoreductase 20 kDa subunit, is a 213 amino acid protein that is suggested to be required for catalytic activity. Defects in the gene encoding NDUFS7 are the cause of Leigh syndrome, a severe neurological disorder that is characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.

Catalogus nummer: BOSSBS-11734R-A555

UOM: 1 * 100 µl

Leverancier: Bioss

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Omschrijving: MAATKOLF 250ML GL/STOP NS14 A KB 1 * 2 ST

Catalogus nummer: HIRS2820286

UOM: 1 * 2 ST

Leverancier: HIRSCHMANN

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