Luciferin is a common bioluminescent reporter used for in vivo imaging of the expression of the luciferase. This substrate for the Firefly luciferase enzyme utilizes ATP and Mg2+ as co-factors and emits a characteristic yellow-green emission in the presence of oxygen, which shifts to red light in vivo at 37°C. DL is a racemic mixture of D-Luciferin and L-Luciferin. DMNPE-caged luciferin can be used to measure intracellular functions since it readily crosses cell membranes. Once it is inside the cell, active luciferin can be released by UV light or by the action of endogenous intracellular esterases. DMNPE-caged luciferin makes it easier to follow the changes in gene expression in live cells. It can also be used in combination with DMNPE-caged ATP. CAS Number: 154140-55-3 Molecular Formula: C21H19N3O7S2 Molecular Weight: 489.517 g/mol InChI Key: KQVRVPOUBLPROI-VXPUYCOJSA-N

Dextran is a polymer of anhydroglucose. It is composed of approximately 95% alpha-D-(166) linkages. The remaining (163) linkages account for the branching of dextran. Dextran sulfate has many applications and when performing nucleic acid hybridizations, may be used as an accelerant to decrease the time required for probe annealing. Dextran sulfate may be included in the hybridization buffer when the rate of hybridization is a limiting factor in detecting rare sequences or it may be included in the hybridization buffer when a limited amount of probe is available. Dextran sulfate functions as an accelerant by excluding the nucleic acid from the volume of solution occupied by the polymer, thereby, increasing the effective probe concentration. CAS Number: 9011-18-1

Dextran is a polymer of anhydroglucose. It is composed of approximately 95% alpha-D-(166) linkages. The remaining (163) linkages account for the branching of dextran. Dextran sulfate has many applications and when performing nucleic acid hybridizations, may be used as an accelerant to decrease the time required for probe annealing. Dextran sulfate may be included in the hybridization buffer when the rate of hybridization is a limiting factor in detecting rare sequences or it may be included in the hybridization buffer when a limited amount of probe is available. Dextran sulfate functions as an accelerant by excluding the nucleic acid from the volume of solution occupied by the polymer, thereby, increasing the effective probe concentration. CAS Number: 9011-18-1

Dextran is a polymer of anhydroglucose. It is composed of approximately 95% alpha-D-(166) linkages. The remaining (163) linkages account for the branching of dextran. Dextran sulfate has many applications and when performing nucleic acid hybridizations, may be used as an accelerant to decrease the time required for probe annealing. Dextran sulfate may be included in the hybridization buffer when the rate of hybridization is a limiting factor in detecting rare sequences or it may be included in the hybridization buffer when a limited amount of probe is available. Dextran sulfate functions as an accelerant by excluding the nucleic acid from the volume of solution occupied by the polymer, thereby, increasing the effective probe concentration. CAS Number: 9011-18-1

Sodium deoxycholate is a bile acid formed by bacterial action from cholate. It is usually conjugated with glycine or taurine. Deoxycholic acid acts as a detergent to solubilize fats for intestinal absorption, is reabsorbed itself, and is used as a choleretic and detergent. CAS Number: 302-95-4; Synonyms: Sodium deoxycholate; Deoxycholic acid sodium salt; Deoxycholate sodium; Desoxycholate sodium; Sodium desoxycholate; Sodium 7-deoxycholate Molecular Formula: C24H39NaO4; Molecular Weight: 414.562 g/mol InChI Key: FHHPUSMSKHSNKW-SMOYURAASA-M

Sodium deoxycholate is a bile acid formed by bacterial action from cholate. It is usually conjugated with glycine or taurine. Deoxycholic acid acts as a detergent to solubilize fats for intestinal absorption, is reabsorbed itself, and is used as a choleretic and detergent. CAS Number: 302-95-4; Synonyms: Sodium deoxycholate; Deoxycholic acid sodium salt; Deoxycholate sodium; Desoxycholate sodium; Sodium desoxycholate; Sodium 7-deoxycholate Molecular Formula: C24H39NaO4; Molecular Weight: 414.562 g/mol InChI Key: FHHPUSMSKHSNKW-SMOYURAASA-M

CAS#: 6104-58-1, Molecular Formula: C47H48N3O7S2Na, MW: 854.04, Coomassie Brilliant Blue G-250 Dye for Gel Protein Stains

CAS#: 6104-58-1, Molecular Formula: C47H48N3O7S2Na, MW: 854.04, Coomassie Brilliant Blue G-250 Dye for Gel Protein Stains

Citrate is a intermediate in the TCA cycle and fatty acid synthesis. Citrate is an allosteric modulator of acetyl-CoA carboxylase, the enzyme that regulates the conversion of acetyl-CoA to malonyl-CoA. It possesses a saline, mildly tart flavor. It is mildly basic and can be used along with citric acid to make biologically compatible buffers. CAS Number: 6132-04-3; Synonyms: Sodium citrate tribasic dihydrate; Trisodium citrate dihydrate; Sodium citrate dihydrate; Molecular Formula: HOC(COONa)(CH2COONa)2 · 2H20; Molecular Weight: 294.10 g/mol InChI Key: NLJMYIDDQXHKNR-UHFFFAOYSA-K

Citrate is a intermediate in the TCA cycle and fatty acid synthesis. Citrate is an allosteric modulator of acetyl-CoA carboxylase, the enzyme that regulates the conversion of acetyl-CoA to malonyl-CoA. It possesses a saline, mildly tart flavor. It is mildly basic and can be used along with citric acid to make biologically compatible buffers. CAS Number: 6132-04-3; Synonyms: Sodium citrate tribasic dihydrate; Trisodium citrate dihydrate; Sodium citrate dihydrate; Molecular Formula: HOC(COONa)(CH2COONa)2 · 2H20; Molecular Weight: 294.10 g/mol InChI Key: NLJMYIDDQXHKNR-UHFFFAOYSA-K

CAS Number: 77-92-9; Synonyms: 2-hydroxypropane-1,2,3-tricarboxylic acid; Citric acid, anhydrous; Citro; Anhydrous citric acid; Molecular Formula: CH2COOH-C(OH)COOH-CH2COOH; Molecular Weight: 192.123 g/mol InChI Key: KRKNYBCHXYNGOX-UHFFFAOYSA-N

CAS Number: 77-92-9; Synonyms: 2-hydroxypropane-1,2,3-tricarboxylic acid; Citric acid, anhydrous; Citro; Anhydrous citric acid; Molecular Formula: CH2COOH-C(OH)COOH-CH2COOH; Molecular Weight: 192.123 g/mol InChI Key: KRKNYBCHXYNGOX-UHFFFAOYSA-N

Reversible blocking of primary amines and reactive towards primary amines. Versatile reagent used for the synthesis of maleimides, bicyclic pyrrolidines, and co- and terpolymers, as well as for the protection of N-terminal amino acids. CAS Number: 616-02-4; Synonyms: 3-methylfuran-2,5-dione; 2-Methylmaleic anhydride; 2,5-Furandione, 3-methyl-; METHYLMALEIC ANHYDRIDE; Molecular Formula: C5H4O3; Molecular Weight: 112.084 g/mol (anhydrous basis) InChI Key: AYKYXWQEBUNJCN-UHFFFAOYSA-N

Reversible blocking of primary amines and reactive towards primary amines. Versatile reagent used for the synthesis of maleimides, bicyclic pyrrolidines, and co- and terpolymers, as well as for the protection of N-terminal amino acids. CAS Number: 616-02-4; Synonyms: 3-methylfuran-2,5-dione; 2-Methylmaleic anhydride; 2,5-Furandione, 3-methyl-; METHYLMALEIC ANHYDRIDE; Molecular Formula: C5H4O3; Molecular Weight: 112.084 g/mol (anhydrous basis) InChI Key: AYKYXWQEBUNJCN-UHFFFAOYSA-N

CAS No.: 4430-20-0 Molecular Formula:C19H12Cl2O5S MW:423.270

CAS No.: 4430-20-0 Molecular Formula: C19H12Cl2O5S MW:423.270

Chloramphenicol is a semisynthetic, broad-spectrum antibiotic derived from Streptomyces venequelae with primarily bacteriostatic activity. Chloramphenicol diffuses through the bacterial cell wall and reversibly binds to the bacterial 50S ribosomal subunit. The binding interferes with peptidyl transferase activity, thereby prevents transfer of amino acids to the growing peptide chains and blocks peptide bond formation. As a result, bacterial protein synthesis is blocked and impede bacterial cell proliferation. CAS Number: 56-75-7; Synonyms: Chloromycetin; Chlornitromycin; Chlorocid; Levomycetin; Molecular Formula: C11H12Cl2N2O5 Molecular Weight: 323.126 g/mol InChI Key: WIIZWVCIJKGZOK-RKDXNWHRSA-N

Chloramphenicol is a semisynthetic, broad-spectrum antibiotic derived from Streptomyces venequelae with primarily bacteriostatic activity. Chloramphenicol diffuses through the bacterial cell wall and reversibly binds to the bacterial 50S ribosomal subunit. The binding interferes with peptidyl transferase activity, thereby prevents transfer of amino acids to the growing peptide chains and blocks peptide bond formation. As a result, bacterial protein synthesis is blocked and impede bacterial cell proliferation. CAS Number: 56-75-7; Synonyms: Chloromycetin; Chlornitromycin; Chlorocid; Levomycetin; Molecular Formula: C11H12Cl2N2O5 Molecular Weight: 323.126 g/mol InChI Key: WIIZWVCIJKGZOK-RKDXNWHRSA-N

A non denaturing zwitterionic detergent with characteristics similar to CHAPS, although more soluble due to a more polar head group. Useful for the solubilization of integral membrane proteins. CHAPSO has been used in a study to assess the processes of liposome solubilization and reconstitution of two transport proteins. It has also been used in a study to investigate a novel bicelle system for orienting macromolecules over a wide temperature range. It can be used for solubilization of membrane proteins. Both CHAPS and CHAPSO have low light absorbance in the ultraviolet region of the electromagnetic spectrum, which is useful for monitoring ongoing chemical reactions or protein-protein binding with UV/Vis spectroscopy. CAS Number: 82473-24-3; Synonyms: MFCD00081079; CHAPS Hydroxy analog; BioXtra; AC1L3U2M; 3-((3-Cholamidopropyl)dimethylammonio)-2-hydroxy-1-propanesulfonate; Molecular Formula: C32H58N2O8S Molecular Weight: 630.882 g/mol (anhydrous basis) InChI Key: GUQQBLRVXOUDTN-XOHPMCGNSA-N

CHAPS is a zwitterionic surfactant used in the laboratory to solubilize biological macromolecules such as proteins. It has both hydrophilic and hydrophobic properties. It can be used for s olubilization of membrane proteins. Combines the properties of both the sulfobetaine-type and bile-acid detergents. Both CHAPS and CHAPSO have low light absorbance in the ultraviolet region of the electromagnetic spectrum, which is useful for monitoring ongoing chemical reactions or protein-protein binding with UV/Vis spectroscopy. CAS Number: 75621-03-3; Synonyms: CHEBI:1418; 3-((3-Cholamidopropyl)dimethylammonium)-1-propanesulfonate; Molecular Formula: C32H58N2O7S Molecular Weight: 614.883 g/mol (anhydrous basis) InChI Key: UMCMPZBLKLEWAF-BCTGSCMUSA-N