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Filtered Search Results
Gibco™ Penicillin-Streptomycin (10,000 U/mL)
For prevention of bacterial contamination of cell cultures due to their effective combined action against gram-positive and gram-negative bacteria
| Sterilization Method | Sterile-filtered |
|---|---|
| Product Type | Antibiotic |
| Form | Liquid |
| Shelf Life | 12 Months |
| Concentration | 100 X |
| For Use With (Application) | Prevention of Cell Culture Contamination |
| Sterility | Sterile-filtered |
Ampicillin sodium salt
CAS: 69-52-3 Molecular Formula: C16H21N3NaO4S Molecular Weight (g/mol): 374.411 MDL Number: MFCD00064313 InChI Key: BSFVNXCYXDYHOD-ZQDFAFASSA-N PubChem CID: 131673879 IUPAC Name: (2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;molecular hydrogen;sodium SMILES: [HH].CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C.[Na]
| PubChem CID | 131673879 |
|---|---|
| CAS | 69-52-3 |
| Molecular Weight (g/mol) | 374.411 |
| MDL Number | MFCD00064313 |
| SMILES | [HH].CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C.[Na] |
| IUPAC Name | (2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;molecular hydrogen;sodium |
| InChI Key | BSFVNXCYXDYHOD-ZQDFAFASSA-N |
| Molecular Formula | C16H21N3NaO4S |
Gibco™ Kanamycin Sulfate
Water-soluble antibiotic originally purified from bacterium Streptomyces kanamyceticus
| Product Type | Antibiotic |
|---|---|
| For Use With (Application) | Bacterial Selection |
Ampicillin Sodium Salt (Crystalline Powder), Fisher BioReagents™
CAS: 69-52-3 Molecular Formula: C16H21N3NaO4S Molecular Weight (g/mol): 374.411 InChI Key: BSFVNXCYXDYHOD-ZQDFAFASSA-N Synonym: Ampicillin PubChem CID: 131673879 IUPAC Name: (2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;molecular hydrogen;sodium SMILES: [HH].CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C.[Na]
| PubChem CID | 131673879 |
|---|---|
| CAS | 69-52-3 |
| Molecular Weight (g/mol) | 374.411 |
| SMILES | [HH].CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C.[Na] |
| Synonym | Ampicillin |
| IUPAC Name | (2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;molecular hydrogen;sodium |
| InChI Key | BSFVNXCYXDYHOD-ZQDFAFASSA-N |
| Molecular Formula | C16H21N3NaO4S |
Kanamycin Sulfate (White Powder), Fisher BioReagents
For selecting transformed cells containing kanamycin resistance gene | CAS: 25389-94-0 | C18H38N4O15S | 582.575 g/mol
Penicillin G sodium salt
CAS: 69-57-8 Molecular Formula: C16H17N2NaO4S Molecular Weight (g/mol): 356.372 MDL Number: MFCD00069666 InChI Key: FCPVYOBCFFNJFS-LQDWTQKMSA-M Synonym: Benzylpenicillin sodium salt PubChem CID: 23668834 ChEBI: CHEBI:51765 IUPAC Name: sodium;(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)[O-])C.[Na+]
| PubChem CID | 23668834 |
|---|---|
| CAS | 69-57-8 |
| Molecular Weight (g/mol) | 356.372 |
| ChEBI | CHEBI:51765 |
| MDL Number | MFCD00069666 |
| SMILES | CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)[O-])C.[Na+] |
| Synonym | Benzylpenicillin sodium salt |
| IUPAC Name | sodium;(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate |
| InChI Key | FCPVYOBCFFNJFS-LQDWTQKMSA-M |
| Molecular Formula | C16H17N2NaO4S |
Tetracycline hydrochloride, 96%
CAS: 64-75-5 Molecular Formula: C22H25ClN2O8 Molecular Weight (g/mol): 480.898 MDL Number: MFCD00078142 InChI Key: HTXDZWDXSWLLLW-FMZCEJRJSA-N PubChem CID: 129628373 IUPAC Name: (4S,4aS,5aS,6S,12aS)-4-(dimethylamino)-3,6,10,11,12a-pentahydroxy-6-methyl-1,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide;hydrochloride SMILES: CC1(C2CC3C(C(=C(C(=O)C3(C(=O)C2=C(C4=C1C=CC=C4O)O)O)C(=O)N)O)N(C)C)O.Cl
| PubChem CID | 129628373 |
|---|---|
| CAS | 64-75-5 |
| Molecular Weight (g/mol) | 480.898 |
| MDL Number | MFCD00078142 |
| SMILES | CC1(C2CC3C(C(=C(C(=O)C3(C(=O)C2=C(C4=C1C=CC=C4O)O)O)C(=O)N)O)N(C)C)O.Cl |
| IUPAC Name | (4S,4aS,5aS,6S,12aS)-4-(dimethylamino)-3,6,10,11,12a-pentahydroxy-6-methyl-1,12-dioxo-4,4a,5,5a-tetrahydrotetracene-2-carboxamide;hydrochloride |
| InChI Key | HTXDZWDXSWLLLW-FMZCEJRJSA-N |
| Molecular Formula | C22H25ClN2O8 |
Gibco™ Geneticin™ Selective Antibiotic (G418 Sulfate) (50 mg/mL)
Produced by bacterium Micromonospora rhodorangea and acts by binding ribosome, thus inhibiting protein synthesis in both prokaryotic and eukaryotic cells
| Product Type | Antibiotic |
|---|---|
| Form | Liquid |
| For Use With (Application) | Eukaryotic Selection/Stable Cell Line Generation |
Thermo Scientific Chemicals Kanamycin sulfate
CAS: 25389-94-0 Molecular Formula: C18H38N4O15S Molecular Weight (g/mol): 582.575 MDL Number: MFCD00070253 InChI Key: OOYGSFOGFJDDHP-IZQIRFRQSA-N PubChem CID: 134129479 IUPAC Name: (2R,3S,4S,5S,6R)-2-(aminomethyl)-6-[(1R,2S,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5R,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol;sulfuric acid SMILES: C1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)O)O)OC3C(C(C(C(O3)CO)O)N)O)N.OS(=O)(=O)O
| PubChem CID | 134129479 |
|---|---|
| CAS | 25389-94-0 |
| Molecular Weight (g/mol) | 582.575 |
| MDL Number | MFCD00070253 |
| SMILES | C1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)O)O)OC3C(C(C(C(O3)CO)O)N)O)N.OS(=O)(=O)O |
| IUPAC Name | (2R,3S,4S,5S,6R)-2-(aminomethyl)-6-[(1R,2S,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5R,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol;sulfuric acid |
| InChI Key | OOYGSFOGFJDDHP-IZQIRFRQSA-N |
| Molecular Formula | C18H38N4O15S |
Cytiva HyClone™ Penicillin Streptomycin 100X Solution
Used to control/destroy destructive microorganisms such as bacteria
Puromycin dihydrochloride, 98%
CAS: 58-58-2 Molecular Formula: C22H31Cl2N7O5 Molecular Weight (g/mol): 544.43 MDL Number: MFCD00150080 InChI Key: MKSVFGKWZLUTTO-MLYJQVMKNA-N PubChem CID: 131632508 SMILES: Cl.Cl.COC1=CC=C(C[C@H](N)C(=O)N[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C(N=CN=C23)N(C)C)C=C1
| PubChem CID | 131632508 |
|---|---|
| CAS | 58-58-2 |
| Molecular Weight (g/mol) | 544.43 |
| MDL Number | MFCD00150080 |
| SMILES | Cl.Cl.COC1=CC=C(C[C@H](N)C(=O)N[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O)N2C=NC3=C(N=CN=C23)N(C)C)C=C1 |
| InChI Key | MKSVFGKWZLUTTO-MLYJQVMKNA-N |
| Molecular Formula | C22H31Cl2N7O5 |
Kanamycin Sulfate, Ultrapure
CAS: 25389-94-0 Molecular Formula: C18H38N4O15S Molecular Weight (g/mol): 582.575 MDL Number: MFCD00070253 InChI Key: OOYGSFOGFJDDHP-IZQIRFRQSA-N Synonym: Kanamycin A PubChem CID: 134129479 IUPAC Name: (2 R,3 S,4 S,5 S,6 R)-2-(aminomethyl)-6-[(1 R,2 S,3 S,4 R,6 S)-4,6-diamino-3-[(2 S,3 R,4 S,5 R,6 R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol;sulfuric acid SMILES: C1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)O)O)OC3C(C(C(C(O3)CO)O)N)O)N.OS(=O)(=O)O
| PubChem CID | 134129479 |
|---|---|
| CAS | 25389-94-0 |
| Molecular Weight (g/mol) | 582.575 |
| MDL Number | MFCD00070253 |
| SMILES | C1C(C(C(C(C1N)OC2C(C(C(C(O2)CN)O)O)O)O)OC3C(C(C(C(O3)CO)O)N)O)N.OS(=O)(=O)O |
| Synonym | Kanamycin A |
| IUPAC Name | (2 R,3 S,4 S,5 S,6 R)-2-(aminomethyl)-6-[(1 R,2 S,3 S,4 R,6 S)-4,6-diamino-3-[(2 S,3 R,4 S,5 R,6 R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxyoxane-3,4,5-triol;sulfuric acid |
| InChI Key | OOYGSFOGFJDDHP-IZQIRFRQSA-N |
| Molecular Formula | C18H38N4O15S |
Gibco™ Gentamicin (10 mg/mL)
Water-soluble antibiotic drug originally purified from the fungus Micromonospora purpurea
| Shipping Condition | Room Temperature |
|---|---|
| Content And Storage | Storage conditions: 15-30°C Shipping conditions: Ambient Shelf life: 24 months from date of manufacture |
| Product Type | Antibiotic |
| Form | Liquid |
| Culture Type | Mammalian Cell Culture |
| Shelf Life | 24 Months |
| Concentration | 10 mg/mL |
| For Use With (Application) | Prevention of Cell Culture Contamination |
| Sterility | Sterile-filtered |
Gibco™ Penicillin-Streptomycin (5,000 U/mL)
For prevention from bacterial contamination of cell cultures due to their effective combined action against gram-positive and gram-negative bacteria.