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2,5-Dimethoxybenzyl+alcohol
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2,5-Dimethoxybenzyl+alcohol
Catalog Number:
(10262-678)
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.
Catalog Number:
(10262-676)
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.
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
Catalog Number:
(10282-360)
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.
Supplier:
TCI America
Description:
CAS Number: 505-10-2
MDL Number: MFCD00036560 Molecular Formula: C4H10OS Molecular Weight: 106.18 Purity/Analysis Method: >99.0% (GC) Form: Clear Liquid Boiling point (°C): 136 Flash Point (°C): 87 Specific Gravity (20/20): 1.03
Catalog Number:
(TCM2215-5G)
Supplier:
TCI America
Description:
(R)-(-)-A-Methoxy-A-(trifluoromethyl)phenylacetyl Chloride, CAS Number: 39637-99-5, MF: C10H8ClF3O, Molecular Weight: 252.62, Synonyms: (-)-Moshers Acid Chloride (ca. 18% in Dichloromethane, ca. 1.0mol/L), (R)-(-)-MTPA-Cl, Size: 5G
Catalog Number:
(76010-908)
Supplier:
Prosci
Description:
This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols by utilizing NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme catalyzes the reduction of prostaglandin (PG) D2, PGH2 and phenanthrenequinone (PQ), and the oxidation of 9alpha,11beta-PGF2 to PGD2. It may play an important role in the pathogenesis of allergic diseases such as asthma, and may also have a role in controlling cell growth and/or differentiation. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14.
Supplier:
Spectrum Chemicals
Description:
Sorbitol, Powder, FCC is used is as a sugar substitute sweetener in many foods. The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.
Supplier:
AMBEED, INC
Description:
(3-Amino-4-fluorophenyl)methanol, Purity: 98%, CAS number: 227609-86-1, Appearance: White to Yellow Solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1G
Supplier:
Diagnostic Biosystems
Description:
PermaBlue Plus/AP is a substrate-chromogen system designed to be used for either IHC or ISH when utilizing alkaline phosphatase
Catalog Number:
(TCM0170-025ML)
Supplier:
TCI America
Description:
CAS Number: 1565-80-6
MDL Number: MFCD00064299 Molecular Formula: C5H12O Molecular Weight: 88.15 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Boiling point (°C): 128 Flash Point (°C): 43 Specific Gravity (20/20): 0.82 Specific rotation [a]20/D: -5.5 deg (neat)
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
Supplier:
MP Biomedicals
Description:
D-Tryptophan is an amino acid and a unnatural isomer of tryptophan.
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:
(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.
Supplier:
Omega Bio-Tek
Description:
The E.Z.N.A.® Plasmid Midi Kit offers a novel and reliable method of isolating up to 200µg of plasmid DNA in less than 60 minutes
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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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