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Methyl-2-aminothiazole-5-carboxylate
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Methyl-2-aminothiazole-5-carboxylate
Catalog Number:
(700009-484)
Supplier:
Spectrum Chemicals
Description:
Asiaticoside is used to study potential treatments for wounds and burns. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.
Supplier:
Matrix Scientific
Description:
MF=C7H7NO2 MW=137.14 CAS=4021-08-3 MDL=MFCD03731175 1G
Supplier:
AMBEED, INC
Description:
3-Methylbenzofuran-2-carboxylic acid, Purity: 98%, CAS Number: 24673-56-1, Appearance: Beige to Yellow Solid, Storage: Sealed in dry, Room Temperature, Size: 10G
Catalog Number:
(TCN0490-025G)
Supplier:
TCI America
Description:
CAS Number: 389-08-2
MDL Number: MFCD00006884 Molecular Formula: C12H12N2O3 Molecular Weight: 232.24 Purity/Analysis Method: >95.0% (T) Form: Crystal Melting point (°C): 229
Supplier:
Enzo Life Sciences
Description:
Cell-permeable, potent, selective, and ATP-competitive mTOR inhibitor.
Supplier:
MP Biomedicals
Description:
Amphotericin B is a polyene antifungal antibiotic from Streptomyces. It has an affinity for sterols, primarily ergosterols, of fungal cell membranes. It forms channels in the membranes, causing small molecules to leak out which contributes to cell death.
Catalog Number:
(10802-270)
Supplier:
Rockland Immunochemical
Description:
Until recently, 5-methylcytosine (5-mC) was the only known modification of DNA for epigenetic regulation. In 2009, however, a second methylated cytosine, 5-hydroxymethylcytosine (5-hmC) was discovered. This new modified base (also called the Sixth base) is generated by enzymatic conversion of 5-mC into 5-hmC by the TET family of oxygenases. Recent results indicate that 5-hmC plays important roles distinct from 5-mC. Although its precise role has still to be shown, early evidence suggests that 5-hmC may well represent a new pathway to demethylate DNA involving a repair mechanism converting 5-hmC to cytosine. This pathway could involve further oxidation of the hydroxymethyl group to a formyl or carboxyl group followed by either deformylation or decarboxylation. The carboxyl and formyl groups of 5-Formylcytosine (5-fC) and 5-Carboxylcytosine (5-caC) could be enzymatically removed without excision of the base. Due to their structural similarity, the different modified cytosine analogues are difficult to discriminate. The development of highly specific affinity-based reagents, such as antibodies, appears to be the most powerful way to differentially and specifically enrich 5-mC and 5-hmC sequences. Anti-5caC Antibody is ideal for research in Genetics and Epigenetics.
Supplier:
TCI America
Description:
CAS Number: 42831-50-5
Molecular Formula: C5H5NO3 Molecular Weight: 127.10 Purity/Analysis Method: >98.0% (T,HPLC) Form: Crystal Melting point (°C): 147
Supplier:
AMBEED, INC
Description:
tert-Butyl-3-oxopyrrolidine-1-carboxylate 97%
Supplier:
AMBEED, INC
Description:
(4aS,6aS,6bR,8aR,9R,10S,12aR,12bR,14bS)-(2S,3R,4S,5S,6R)-6-((((2R,3R,4R,5S,6R)-3,4-Dihydroxy-6-(hydroxymethyl)-5-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)methyl)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl, 99+%, CAS: 14216-03-6, Size: 1MG
Supplier:
AMBEED, INC
Description:
4-Methylpicolinic acid 97%
Supplier:
AMBEED, INC
Description:
tert-Butyl-3-iodoazetidine-1-carboxylate 97%
Supplier:
AMBEED, INC
Description:
tert-Butyl-3-hydroxyazetidine-1-carboxylate 98%
Supplier:
AMBEED, INC
Description:
tert-Butyl-3-oxoazetidine-1-carboxylate 98%
Catalog Number:
(PI22360)
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce SMCC is a hetero-bifunctional crosslinker that contain N-hydroxysuccinimide (NHS) ester and maleimide groups that allow covalent conjugation of amine- and sulfhydryl-containing molecules. NHS esters react with primary amines at pH 7–9 to form amide bonds, while maleimides react with sulfhydryl groups at pH 6.5–7.5 to form stable thioether bonds. In aqueous solutions, NHS ester hydrolytic degradation is a competing reaction whose rate increases with pH. The maleimide group is more stable than the NHS-ester group, but will slowly hydrolyze and lose its reaction specificity for sulfhydryls at pH values > 7.5. For these reasons, conjugations with these crosslinkers are usually performed at pH 7.2–7.5, with the NHS ester (amine-targeted) reacted before or simultaneous with the maleimide (sulfhydryl-targeted) reaction.
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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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