You Searched For: 2-Chloro-4-fluorotoluene


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Catalog Number: (10109-202)
Supplier: Prosci
Description: SLC35A3 is a uridine diphosphate-N-acetylglucosamine transporter in the Golgi apparatus.


Catalog Number: (76700-642)
Supplier: AFG Bioscience
Description: Human 2, 3-Diphosphoglycerate, 2, 3-DPG ELISA Kit


Catalog Number: (10206-982)
Supplier: Boster Biological Technology
Description: Rabbit IgG polyclonal antibody for Ribonucleoside-diphosphate reductase subunit M2 B(RRM2B) detection. Tested with WB in Human;Mouse;Rat.


Supplier: AFG Bioscience
Description: 2,​3,​4,​6-​Tetra-​O-​acetyl-​β-​D-​galactopyranosyl PEG3-​azide ≥95%

Supplier: Thermo Scientific Chemicals
Description: Tetra-n-dodecylammonium iodide 98%

Catalog Number: (77438-516)
Supplier: Bioss
Description: ATP + L-methionine + tRNA(Met) = AMP + diphosphate + L-methionyl-tRNA(Met).


Catalog Number: (76080-318)
Supplier: Bioss
Description: PMVK is a 192 amino acid peroxisomal enzyme belonging to the nucleoside monophosphate (NMP) kinase family and is expressed in heart, liver, skeletal muscle, kidney, and pancreas with lower expression in brain, placenta and lung. Induced by sterol, PMVK participates in isopentenyl diphosphate biosynthesis via the mevalonate pathway. PMVK catalyzes the conversion of mevalonate 5-phosphate into mevalonate 5-diphosphate in the fifth reaction of the cholesterol biosynthetic pathway. PMVK exists as a monomer and is encoded by a gene located on human chromosome 1, which houses over 3,000 genes and is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome.


Catalog Number: (10414-300)
Supplier: Bioss
Description: PMVK is a 192 amino acid peroxisomal enzyme belonging to the nucleoside monophosphate (NMP) kinase family and is expressed in heart, liver, skeletal muscle, kidney, and pancreas with lower expression in brain, placenta and lung. Induced by sterol, PMVK participates in isopentenyl diphosphate biosynthesis via the mevalonate pathway. PMVK catalyzes the conversion of mevalonate 5-phosphate into mevalonate 5-diphosphate in the fifth reaction of the cholesterol biosynthetic pathway. PMVK exists as a monomer and is encoded by a gene located on human chromosome 1, which houses over 3,000 genes and is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome.


Catalog Number: (10414-302)
Supplier: Bioss
Description: PMVK is a 192 amino acid peroxisomal enzyme belonging to the nucleoside monophosphate (NMP) kinase family and is expressed in heart, liver, skeletal muscle, kidney, and pancreas with lower expression in brain, placenta and lung. Induced by sterol, PMVK participates in isopentenyl diphosphate biosynthesis via the mevalonate pathway. PMVK catalyzes the conversion of mevalonate 5-phosphate into mevalonate 5-diphosphate in the fifth reaction of the cholesterol biosynthetic pathway. PMVK exists as a monomer and is encoded by a gene located on human chromosome 1, which houses over 3,000 genes and is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome.


Catalog Number: (TCT3288-1G)
Supplier: TCI America
Description: N,N,N',N'-Tetra(2-naphthyl)benzidine, Purity: >98.0%(HPLC)(N), Cas number: 141752-82-1, Molecular Formula: C52H36N2, Molecular Weight: 688.87, Appearance: Very pale yellow - Yellow solid crystal powder, Size: 1G

SDS


Supplier: TCI America
Description: 2,2',6,6'-Tetra-tert-butyl-4,4'-dihydroxybiphenyl, Purity: >98%(GC), CAS: 128-38-1, MF: C28H42O2, MW: 410.64, Synonyms: 2,2',6,6'-Tetra-tert-butyl-[1,1'-biphenyl]-4,4'-diol, Form: Crystal - Powder, Slightly pale yellow - Yellow, Size: 200MG

Catalog Number: (10414-280)
Supplier: Bioss
Description: PMVK is a 192 amino acid peroxisomal enzyme belonging to the nucleoside monophosphate (NMP) kinase family and is expressed in heart, liver, skeletal muscle, kidney, and pancreas with lower expression in brain, placenta and lung. Induced by sterol, PMVK participates in isopentenyl diphosphate biosynthesis via the mevalonate pathway. PMVK catalyzes the conversion of mevalonate 5-phosphate into mevalonate 5-diphosphate in the fifth reaction of the cholesterol biosynthetic pathway. PMVK exists as a monomer and is encoded by a gene located on human chromosome 1, which houses over 3,000 genes and is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome.


Catalog Number: (10396-474)
Supplier: Bioss
Description: This gene encodes the small subunit of a p53-inducible ribonucleotide reductase. This heterotetrameric enzyme catalyzes the conversion of ribonucleoside diphosphates to deoxyribonucleoside diphosphates. The product of this reaction is necessary for DNA synthesis. Mutations in this gene have been associated with autosomal recessive mitochondrial DNA depletion syndrome, autosomal dominant progressive external ophthalmoplegia-5, and mitochondrial neurogastrointestinal encephalopathy. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010].


Catalog Number: (10396-472)
Supplier: Bioss
Description: This gene encodes the small subunit of a p53-inducible ribonucleotide reductase. This heterotetrameric enzyme catalyzes the conversion of ribonucleoside diphosphates to deoxyribonucleoside diphosphates. The product of this reaction is necessary for DNA synthesis. Mutations in this gene have been associated with autosomal recessive mitochondrial DNA depletion syndrome, autosomal dominant progressive external ophthalmoplegia-5, and mitochondrial neurogastrointestinal encephalopathy. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010].


Supplier: TCI America
Description: CAS Number: 64913-16-2
MDL Number: MFCD00069791
Molecular Formula: C14H20O9
Molecular Weight: 332.31
Purity/Analysis Method: >98.0% (HPLC)
Form: Crystal
Color: White
Melting point (°C): 94
Specific rotation [a]20/D: -120 deg (C=1, CHCl3)
Storage Temperature: <0°C

SDS

Catalog Number: (10401-614)
Supplier: Bioss
Description: This gene encodes the small subunit of a p53-inducible ribonucleotide reductase. This heterotetrameric enzyme catalyzes the conversion of ribonucleoside diphosphates to deoxyribonucleoside diphosphates. The product of this reaction is necessary for DNA synthesis. Mutations in this gene have been associated with autosomal recessive mitochondrial DNA depletion syndrome, autosomal dominant progressive external ophthalmoplegia-5, and mitochondrial neurogastrointestinal encephalopathy. Alternatively spliced transcript variants have been described.[provided by RefSeq, Feb 2010].


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