1614 Results for: "RITA&amp"

Supplier: Enzo Life Sciences

Inhibitor of p53/HDM2 interaction

Supplier: Merck

AMP (2-Amino-2-methylpropanol) for synthesis, Sigma-Aldrich®

Supplier: Thermo Fisher Scientific

AMP (2-Amino-2-methylpropanol) 99%

Supplier: Thermo Fisher Scientific

AMP (2-Amino-2-methylpropanol), (max. 5% H₂O) 95%

Supplier: Apollo Scientific

Used for the preparation of buffer solutions, suitable for the determination of alkaline phosphatase.

Supplier: VWR Chemicals

5% water has been added to maintain liquidity at room temperature.

Supplier: Molekula

AMP (2-Amino-2-methylpropanol)

Supplier: Thermo Fisher Scientific

Adenosine-5'-monophosphoric acid (AMP) 99%

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Merck

AMP (2-Amino-2-methylpropanol), Sigma-Aldrich®

Supplier: Thermo Fisher Scientific

a useful ligand determinant that facilitate the binding of APS reductase inhibitors and activates adenosine receptor agonists.

Supplier: Spectrum Chemical

2-Amino-2-methyl-1-propanol, or aminomethyl propanol is a colourless, viscous liquid that functions as a pH adjuster. It is also used as an intermediate in drug synthetic schemes.

Supplier: AAT Bioquest

AMP-Fluorescein conjugate calibrator is desigend to use with AAT Bioquests' green fluorescent FAM-cAMP PDE IV substrate, a cAMP derivative that is a specific substrate for phosphodiesterase (PDE) IV.

Supplier: Enzo Life Sciences

Adenosine 5'-monophosphate disodium salt (AMP disodium salt) ≥98% (by HPLC)

Supplier: Thermo Fisher Scientific

Adenosine 5'-monophosphate disodium salt (AMP disodium salt) hydrate

Supplier: Molekula

Adenosine 5'-monophosphate disodium salt (AMP disodium salt) hydrate

Supplier: Merck

Adenosine 5'-monophosphate disodium salt (AMP disodium salt) hydrate, Sigma-Aldrich®

Supplier: MP Biomedicals

Adenosine 5'-monophosphate disodium salt (AMP disodium salt) hydrate ≥99%, powder

Supplier: Bioss

Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.

Supplier: Apollo Scientific

Adenosine 5'-monophosphate monohydrate ≥96%

Supplier: MP Biomedicals

Adenosine 5′-monophosphate is a nucleotide that is used as a monomer in RNA. It is an ester of phosphoric acid and the nucleoside adenosine. AMP consists of a phosphate group, the sugar ribose, and the nucleobase adenine.

Supplier: Bioss

Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterisation.

Supplier: US Biological

Anti-Cyclic AMP Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-cyclic AMP Rabbit Polyclonal Antibody

Supplier: Enzo Life Sciences

Amp'd® ELISA Signal Amplification Kit provides up to 50-fold increase in sensitivity over traditional ELISAs while detecting lower concentrations of target in samples.

Supplier: Bioss

Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterisation.

Supplier: Enzo Life Sciences

Ultra-sensitive AMP'D® GLP-1 ELISA kit enabling the ability to use less sample to detect levels of human Glucagon-like peptide 1 (7-36) amide, a potent promoter of insulin secretion, a major incretin hormone, and therapeutic for type 2 diabetes.

Supplier: Antibodies.com

Human AMPS ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human AMPS in serum, plasma, tissue homogenates, and other biological fluids.