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CAS: 9008-42-8 Synonym: Protargol
CAS | 9008-42-8 |
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Synonym | Protargol |
Blockieren Sie die unspezifische Antikörperbindung des primären Reagenz mit Epredia™ FITC-Proteinblockierungsmittel (PBA)
CAS: 6226-79-5 Summenformel: C22H12N4Na4O13S4 Molekulargewicht (g/mol): 760.552 MDL-Nummer: MFCD00003892 InChI-Schlüssel: VSXKEUCERCWGKF-STNZDNLRSA-J Synonym: C.I. 27195 PubChem CID: 11320219 IUPAC-Name: Tetranatrium;(4Z)-3-oxo-4-[[2-sulfonato-4-[(4-sulfonatophenyl)diazenyl]phenyl]hydrazinyliden]naphthalen-2,7-Disulfonat SMILES: C1=CC(=CC=C1N=NC2=CC(=C(C=C2)NN=C3C4=C(C=C(C=C4)S(=O)(=O)[O-])C=C(C3=O)S(=O)(=O)[O-])S(=O)(=O)[O-])S(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+]
InChI-Schlüssel | VSXKEUCERCWGKF-STNZDNLRSA-J |
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IUPAC-Name | Tetranatrium;(4Z)-3-oxo-4-[[2-sulfonato-4-[(4-sulfonatophenyl)diazenyl]phenyl]hydrazinyliden]naphthalen-2,7-Disulfonat |
PubChem CID | 11320219 |
CAS | 6226-79-5 |
MDL-Nummer | MFCD00003892 |
Molekulargewicht (g/mol) | 760.552 |
SMILES | C1=CC(=CC=C1N=NC2=CC(=C(C=C2)NN=C3C4=C(C=C(C=C4)S(=O)(=O)[O-])C=C(C3=O)S(=O)(=O)[O-])S(=O)(=O)[O-])S(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+] |
Synonym | C.I. 27195 |
Summenformel | C22H12N4Na4O13S4 |
CAS | 7423-31-6 |
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Summenformel | C30H27BrN2S2 |
CAS: 6104-58-1 Summenformel: C47H48N3NaO7S2 Molekulargewicht (g/mol): 854.025 MDL-Nummer: MFCD00078482 InChI-Schlüssel: RWVGQQGBQSJDQV-UHFFFAOYSA-M Synonym: Coomassie Brilliant Blue G 250; C.I. 42655 PubChem CID: 6328534 IUPAC-Name: Natrium;3-[[4-[(Z)-[4-(4-Ethoxyanilin)Phenyl]-[4-[Ethyl-[(3-Sulfonatophenyl)Methyl]azaniumyliden]-2-Methylcyclohexa-2,5-dien-1-Yliden]Methyl]-N-Ethyl-3-Methylanilin]Methyl]Benzolsulfonat SMILES: CCN(CC1=CC(=CC=C1)S(=O)(=O)[O-])C2=CC(=C(C=C2)C(=C3C=CC(=[N+](CC)CC4=CC(=CC=C4)S(=O)(=O)[O-])C=C3C)C5=CC=C(C=C5)NC6=CC=C(C=C6)OCC)C.[Na+]
InChI-Schlüssel | RWVGQQGBQSJDQV-UHFFFAOYSA-M |
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IUPAC-Name | Natrium;3-[[4-[(Z)-[4-(4-Ethoxyanilin)Phenyl]-[4-[Ethyl-[(3-Sulfonatophenyl)Methyl]azaniumyliden]-2-Methylcyclohexa-2,5-dien-1-Yliden]Methyl]-N-Ethyl-3-Methylanilin]Methyl]Benzolsulfonat |
PubChem CID | 6328534 |
CAS | 6104-58-1 |
MDL-Nummer | MFCD00078482 |
Molekulargewicht (g/mol) | 854.025 |
SMILES | CCN(CC1=CC(=CC=C1)S(=O)(=O)[O-])C2=CC(=C(C=C2)C(=C3C=CC(=[N+](CC)CC4=CC(=CC=C4)S(=O)(=O)[O-])C=C3C)C5=CC=C(C=C5)NC6=CC=C(C=C6)OCC)C.[Na+] |
Synonym | Coomassie Brilliant Blue G 250; C.I. 42655 |
Summenformel | C47H48N3NaO7S2 |
Chemischer Name oder Material | Protein Gel-Loading Dye for SDS-PAGE, 2X |
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ChemAlert-Symbol zur Lagerung | Gray |
Farbe | Violett |
Güte | Elektrophorese |
Physikalische Form | Flüssig |
Concentration or Composition (by Analyte or Components) | Sodium Dodecyl Sulfate (<5%), Glycerol (<12%), Tris (<1.0%), Proprietary Component (<2%), and Water (80%). |
CAS | 7647-01-0 |
Empfohlene Lagerung | RT |
Extinktion | 0.15 to 0.35 AU at 252nm,0.25 to 0.40 AU,0.32 to 0.47 AU |
Tyramide signal amplification is enzyme-mediated detection method that uses catalytic activity of horseradish peroxidase (HRP) to generate high-density labeling of target protein or nucleic acid sequence in situ
Enzyme-mediated detection method uses the catalytic activity of horseradish peroxidase (HRP) to generate high-density labeling of a target protein or nucleic acid sequence in situ
Enzyme-mediated detection method uses the catalytic activity of horseradish peroxidase (HRP) to generate high-density labeling of a target protein or nucleic acid sequence in situ
Tyramide signal amplification is enzyme-mediated detection method that uses catalytic activity of horseradish peroxidase (HRP) to generate high-density labeling of target protein or nucleic acid sequence in situ
Tyramide signal amplification is enzyme-mediated detection method that uses catalytic activity of horseradish peroxidase (HRP) to generate high-density labeling of target protein or nucleic acid sequence in situ
Tyramide signal amplification is enzyme-mediated detection method that uses catalytic activity of horseradish peroxidase (HRP) to generate high-density labeling of target protein or nucleic acid sequence in situ
Tyramide signal amplification is enzyme-mediated detection method that uses catalytic activity of horseradish peroxidase (HRP) to generate high-density labeling of target protein or nucleic acid sequence in situ