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Ethylbenzene degradation

pathways : Ethylbenzene degradation pathways:

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Related Genes to "Ethylbenzene degradation" content :

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Related products :

Catalog number Product name Quantity
orb63165 1-Bromo-3-ethylbenzene 1-Bromo-3-ethylbenzene For research use only. 1 g
30-956 Autophagy is the major intracellular degradation system delivering cytoplasmic components to lysosomes, and it accounts for degradation of most long-lived proteins and some organelles. Cytoplasmic con 0.05 mg
30-957 Autophagy is the major intracellular degradation system delivering cytoplasmic components to lysosomes, and it accounts for degradation of most long-lived proteins and some organelles. Cytoplasmic con 0.05 mg
E05220 Ethylbenzene 500 ML
E05220 Ethylbenzene 5000 ML
14815-52 Ethylbenzene CAS: 100-41-4 25ML
14815-65 Ethylbenzene CAS: 100-41-4 500ML
14815-52 Ethylbenzene 25 ml
14815-65 Ethylbenzene 500 ml
E05220 Ethylbenzene 1000 ML
E05220 Ethylbenzene 500 ML
14815-65 Ethylbenzene 500ML
E05220 Ethylbenzene 1000 ML
E05220 Ethylbenzene 5000 ML
14815-52 Ethylbenzene 25ML
REVOC127 VOC Ethylbenzene 2000 5 x 1ml
3719D0200K ETHYLBENZENE 99 percent FOR SYNTHESIS, CAS: 100-41-4 200LTR
3719D0025k ETHYLBENZENE 99 percent FOR SYNTHESIS, CAS: 100-41-4 25LTR
3719D00500 ETHYLBENZENE 99 percent FOR SYNTHESIS, CAS: 100-41-4 5x500ML
M36859840 1-Bromo-3-ethylbenzene CAS: [2725-82-8] 5 g
M44750995 1-Bromo-4-ethylbenzene CAS: [1585-07-5] 25 g
M34519935 1-Bromo-2-ethylbenzene CAS: [1973-22-4] 25 g
3719D02500 ETHYLBENZENE 99 percent FOR SYNTHESIS, CAS: 100-41-4 2,5LTR
27-171 ERLIN2 plays an important role in the early steps of the endoplasmic reticulum-associated degradation (ERAD) pathway. It is involved in ITPR1 degradation by the ERAD pathway. 0.05 mg
31-050 MDM4 inhibits p53- and p73-mediated cell cycle arrest and apoptosis by binding its transcriptional activation domain. It inhibits degradation of MDM2. It can reverse MDM2-targeted degradation of p53 w 0.05 mg

Pathways :

WP1646: Ethylbenzene degradation
WP349: Synthesis and Degradation of Ketone Bodies
WP101: Synthesis and Degradation of Ketone Bodies
WP172: m-cresol degradation
WP60: Toluene degradation
WP1633: Bisphenol A degradation
WP181: P-cymene Degradation
WP841: Proteasome Degradation
WP432: Asparagine degradation
WP1134: Synthesis and Degradation of Ketone Bodies
WP46: Methionine Degradation
WP1451: Valine, leucine and isoleucine degradation
WP2231: Degradation of apoptotic cells
WP99: Glutamate degradation VIII
WP1654: gamma-Hexachlorocyclohexane degradation
WP1673: Naphthalene and anthracene degradation
WP519: Proteasome Degradation
WP1613: 1,4-Dichlorobenzene degradation
WP281: Proteasome Degradation
WP1623: Atrazine degradation
WP311: Synthesis and Degradation of Ketone Bodies
WP1706: Synthesis and degradation of ketone bodies
WP546: Lactose degradation
WP1717: Valine, leucine and isoleucine degradation
WP573: Phenylalanine Degradation

Related Genes :
Bibliography :
[35768427] Heat-fueled enzymatic cascade for selective oxyfunctionalization of hydrocarbons.
[35724516] Synthetic Saccharomyces cerevisiae tolerate and degrade highly pollutant complex hydrocarbon mixture.
[35684440] The Dual Function of PhOH Included in the Coordination Sphere of the Nickel Complexes in the Processes of Oxidation with Dioxygen.
[35461099] Microbial bioremediation of produced water under different redox conditions in marine sediments.
[35454149] Enhancement of Methane Catalysis Rates in OB3b.
[35439686] Anaerobic degradation of benzene and other aromatic hydrocarbons in a tar-derived plume: Nitrate versus iron reducing conditions.
[35322964] Investigation of kidney function changes in sea salt workers during harvest season in Thailand.
[35305487] Microbial compositional and functional traits of BTEX and salinity co-contaminated shallow groundwater by produced water.
[35138241] sp. nov., a novel aromatic hydrocarbon-degrading bacterium isolated from benzene-, and xylene-degrading enrichment cultures, and emended description of the genus .
[35113105] Aerobic BTEX biodegradation increases yield of perfluoroalkyl carboxylic acids from biotransformation of a polyfluoroalkyl surfactant, 6:2 FtTAoS.