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3-(4-Fluorophenyl)phenethyl+alcohol
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3-(4-Fluorophenyl)phenethyl+alcohol
Catalog Number:
(TCT1997-5G)
Supplier:
TCI America
Description:
CAS Number: 86259-87-2
MDL Number: MFCD06797175 Molecular Formula: C15H24O5 Molecular Weight: 284.35 Purity/Analysis Method: >95.0% (GC) Form: Clear Liquid Color: Very Pale Yellow Specific Gravity (20/20): 1.10
Catalog Number:
(10282-214)
Supplier:
Bioss
Description:
AGPS is a 658 amino acid enzyme that is required for glycerolipid metabolism and ether lipid biosynthesis. Localized to the inner aspect of the peroxisomal membrane, AGPS is likely part of a heterotrimeric complex that is also composed of GNPAT and a modified form of GNPAT. Containing one FAD-binding PCMH-type domain, AGPS utilizes FAD as a cofactor in the synthesis of alkyl-glycerone 3-phophate and a long-chain acid anion from 1-acteyl-glyerone 3-phosphate and a long-chain alcohol. Defects in the gene encoding AGPS results in rhizomelic chondrodysplasia punctata type 3, a disease characterized by vertebral disorders, severe mental retardation, cutaneous lesions, cataracts and rhizomelic shortening of the humerus and femur.
Catalog Number:
(10282-212)
Supplier:
Bioss
Description:
AGPS is a 658 amino acid enzyme that is required for glycerolipid metabolism and ether lipid biosynthesis. Localized to the inner aspect of the peroxisomal membrane, AGPS is likely part of a heterotrimeric complex that is also composed of GNPAT and a modified form of GNPAT. Containing one FAD-binding PCMH-type domain, AGPS utilizes FAD as a cofactor in the synthesis of alkyl-glycerone 3-phophate and a long-chain acid anion from 1-acteyl-glyerone 3-phosphate and a long-chain alcohol. Defects in the gene encoding AGPS results in rhizomelic chondrodysplasia punctata type 3, a disease characterized by vertebral disorders, severe mental retardation, cutaneous lesions, cataracts and rhizomelic shortening of the humerus and femur.
Catalog Number:
(TCT0056-25G)
Supplier:
TCI America
Description:
CAS Number: 2052-49-5
MDL Number: MFCD00009425 Molecular Formula: C16H37NO Molecular Weight: 259.48 Form: Clear Liquid Color: Very Pale Yellow Storage Temperature: 0-10°C
Supplier:
MP Biomedicals
Description:
Glycerol is a simple polyol compound.
Glycerol is used both in sample preparation and gel formation for polyacrylamide gel electrophoresis. Glycerol (5-10%) increases the density of a sample so that the sample will layer at the bottom of a gel’s sample well. Glycerol is also used to aid in casting gradient gels and as a protein stabilizer and storage buffer component. It is used in the concentration and storage of enzymes and also prevents back-diffusion of protein samples into the buffer.
Supplier:
Thermo Scientific Chemicals
Description:
1900.Powder,CAUTION: May irritate skin and eyes,500g,100g.
Catalog Number:
(TCM0171-25ML)
Supplier:
TCI America
Description:
CAS Number: 598-75-4
MDL Number: MFCD00004527 Molecular Formula: C5H12O Molecular Weight: 88.15 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 112 Flash Point (°C): 39 Specific Gravity (20/20): 0.82
Catalog Number:
(76339-780)
Supplier:
New England Biolabs (NEB)
Description:
The Monarch® gDNA Binding Buffer a component of the Monarch® Genomic DNA Purification Kit (NEB #T3010), which can be used to purify up to 30 µg genomic DNA from a variety of sample type.
Supplier:
TCI America
Description:
CAS Number: 100-53-8
MDL Number: MFCD00004867 Molecular Formula: C7H8S Molecular Weight: 124.20 Purity/Analysis Method: >96.0% (GC) Form: Clear Liquid Color: Colorless Boiling point (°C): 195 Melting point (°C): -30 Flash Point (°C): 70 Specific Gravity (20/20): 1.06
Supplier:
MP Biomedicals
Description:
Lecithin is a phosphatidylcholine of soybean origin.
Catalog Number:
(TCH1043-1G)
Supplier:
TCI America
Description:
CAS Number: 24342-68-5
MDL Number: MFCD06797107 Molecular Formula: C19H32O7 Molecular Weight: 372.46 Purity/Analysis Method: >93.0% (GC) Form: Clear Liquid
Catalog Number:
(10073-256)
Supplier:
Prosci
Description:
The NMDA receptor (NMDAR) plays an essential role in memory, neuronal development and it has also been implicated in several disorders of the central nervous system including Alzheimer’s, epilepsy and ischemic neuronal cell death (Grosshans et al., 2002; Wenthold et al., 2003; Carroll and Zukin, 2002). The NMDA receptor is also one of the principal molecular targets for alcohol in the CNS (Lovinger et al., 1989; Alvestad et al., 2003; Snell et al., 1996). The NMDAR is also potentiated by protein phosphorylation (Lu et al., 1999). The rat NMDAR1 (NR1) was the first subunit of the NMDAR to be cloned. The NR1 protein can form NMDA activated channels when expressed in Xenopus oocytes but the currents in such channels are much smaller than those seen in situ. Channels with more physiological characteristics are produced when the NR1 subunit is combined with one or more of the NMDAR2 (NR2 A-D) subunits.
Catalog Number:
(10282-372)
Supplier:
Bioss
Description:
The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. ANKK1 (ankyrin repeat and kinase domain containing 1), also known as PKK2 or SGK288, is a 765 amino acid protein that belongs to the Ser/Thr protein kinase family and contains 12 ANK repeats and one protein kinase domain. Highly expressed in brain tissue and present in lower amounts in placenta and spinal cord, ANKK1 functions to catalyze the ATP-dependent phosphorylation of target proteins and is thought to play a role in alcohol and nicotine dependence. The gene encoding ANKK1 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome.
Catalog Number:
(10282-378)
Supplier:
Bioss
Description:
The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. ANKK1 (ankyrin repeat and kinase domain containing 1), also known as PKK2 or SGK288, is a 765 amino acid protein that belongs to the Ser/Thr protein kinase family and contains 12 ANK repeats and one protein kinase domain. Highly expressed in brain tissue and present in lower amounts in placenta and spinal cord, ANKK1 functions to catalyze the ATP-dependent phosphorylation of target proteins and is thought to play a role in alcohol and nicotine dependence. The gene encoding ANKK1 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome.
Catalog Number:
(10266-758)
Supplier:
Bioss
Description:
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.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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