Esta buscando: 6-Dehydronandrolone+Acetate


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Descripción: 2,6-Dibromopiridina 98%
Numero del catalogo: ACRO112910250
UOM: 1 * 25 g
Proveedor: Thermo Fisher Scientific

FDS


Descripción: 2,5-Dibromopiridina 97%
Numero del catalogo: ACRO112900500
UOM: 1 * 50 g
Proveedor: Thermo Fisher Scientific

FDS


Descripción: 2,4-Dibromopiridina 97%
Numero del catalogo: APOSOR8632-25G
UOM: 1 * 25 g
Proveedor: Apollo Scientific


Descripción: 2,3-Dibromopiridina ≥97%
Numero del catalogo: L19527.14
UOM: 1 * 25 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Descripción: 2,6-Dibromopiridina ≥98%
Numero del catalogo: A15397.36
UOM: 1 * 500 g
Proveedor: Thermo Fisher Scientific

FDS Certificados


Descripción: 2,5-Dibromopiridina ≥99.0% (por GC)
Numero del catalogo: TCIAD1217-25G
UOM: 1 * 25 g
Proveedor: TCI


Descripción: 2,6-Dibromoisonicotinic acid
Numero del catalogo: APOSOR2261-250MG
UOM: 1 * 250 mg
Proveedor: Apollo Scientific


Descripción: Methyl 2,6-dibromoisonicotinate
Numero del catalogo: APOSOR18036-5G
UOM: 1 * 5 g
Proveedor: Apollo Scientific


Descripción: 5,6-Dibromo-2-pyridinamine 97%
Numero del catalogo: APOSOR301215-5G
UOM: 1 * 5 g
Proveedor: Apollo Scientific


Descripción: Thiazolyl Blue Tetrazolium Blue (MTT) may be used in measurement of cell proliferation. MTT produces a yellowish solution that is converted to dark blue, water-insoluble MTT formazan by mitochondrial dehydrogenases of living cells. The blue crystals are solubilized with acidified isopropanol and the intensity is measured colorimetrically at 570 nm. MTT has been used as a histochemical/cytochemical reagent and for the detection of NAD. ADP-linked enzyme systems in tissue cannot be detected with MTT, due to binding of the cation by the cyanide trap used. MTT is rapidly reduced to the formazan, which chelates with nickel, copper, and cobalt; the cobalt chelate has been used in oxidative systems.
Numero del catalogo: M2128-500MG
UOM: 1 * 500 mg
Proveedor: SIGMA ALDRICH MICROSCOPY


Descripción: 2,5-Dibromo-3,4-pyridinediamine
Numero del catalogo: APOSOR302039-1G
UOM: 1 * 1 g
Proveedor: Apollo Scientific


Descripción: Aldehyde dehydrogenases (ALDHs) mediate NADP+-dependent oxidation of aldehydes into acids during the detoxification of alcohol-derived acetaldehyde; metabolism of corticosteroids, biogenic amines and neurotransmitters; and lipid peroxidation. ALDH1A1, also designated retinal dehydrogenase 1 (RalDH1 or RALDH1), aldehyde dehydrogenase family 1 member A1, aldehyde dehydrogenase cytosolic, ALDHII, ALDH-E1 or ALDH E1, is a retinal dehydrogenase that participates in the biosynthesis of retinoic acid (RA). There are two major liver isoforms of ALDH1 that can localize to cytosolic or mitochondrial space. The ALDH1A2 (RALDH2, RALDH2-T) gene produces three different transcripts and also catalyzes the synthesis of RA from retinaldehyde. ALDH1A3 (ALDH6, RALDH3, ALDH1A6) is a 37 kb gene that consists of 13 exons and produces a major transcript of approximately 3.5 kb most abundant in salivary gland, stomach and kidney. ALDH3A1 (stomach type, ALDH3, ALDHIII) forms a cytoplasmic homodimer that preferentially oxidizes aromatic aldehyde substrates. ALDH genes upregulate as a part of the oxidative stress response, and appear to be abundant in certain tumors that have an accelerated metabolism toward chemotherapy agents.
Numero del catalogo: BOSSBS-12460R
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: 2,3-Dibromoisonicotinic acid ≥97%
Numero del catalogo: H31708.03
UOM: 1 * 1 g
Proveedor: Thermo Fisher Scientific

FDS


Descripción: 2,5-Dibromo-4-pyridinylboronic acid
Numero del catalogo: APOSOR110029-1G
UOM: 1 * 1 g
Proveedor: Apollo Scientific


Descripción: Aldehyde dehydrogenases (ALDHs) mediate NADP+-dependent oxidation of aldehydes into acids during the detoxification of alcohol-derived acetaldehyde; metabolism of corticosteroids, biogenic amines and neurotransmitters; and lipid peroxidation. ALDH1A1, also designated retinal dehydrogenase 1 (RalDH1 or RALDH1), aldehyde dehydrogenase family 1 member A1, aldehyde dehydrogenase cytosolic, ALDHII, ALDH-E1 or ALDH E1, is a retinal dehydrogenase that participates in the biosynthesis of retinoic acid (RA). There are two major liver isoforms of ALDH1 that can localize to cytosolic or mitochondrial space. The ALDH1A2 (RALDH2, RALDH2-T) gene produces three different transcripts and also catalyzes the synthesis of RA from retinaldehyde. ALDH1A3 (ALDH6, RALDH3, ALDH1A6) is a 37 kb gene that consists of 13 exons and produces a major transcript of approximately 3.5 kb most abundant in salivary gland, stomach and kidney. ALDH3A1 (stomach type, ALDH3, ALDHIII) forms a cytoplasmic homodimer that preferentially oxidizes aromatic aldehyde substrates. ALDH genes upregulate as a part of the oxidative stress response, and appear to be abundant in certain tumors that have an accelerated metabolism toward chemotherapy agents.
Numero del catalogo: BOSSBS-12460R-HRP
UOM: 1 * 100 µl
Proveedor: Bioss


Descripción: 2,6-Dibromo-3-piridona ≥97.0% (by titrimetric analysis)
Numero del catalogo: TCIAD5174-1G
UOM: 1 * 1 g
Proveedor: TCI


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