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For purification of this Albumin an extensive heat-shock/diafiltration method is used, which has been shown to bring more highly purified products than the standard process acc. to Cohn. The process is taking place in a closed system. Molar extinction coefficient: 4,4x10 4 L x mol -1 x cm -1 (acc. to 0,667 L x mol -1 x cm -1 for a 0,1 % solution). Bovine Serum Albumin (BSA) Fraction V, NZ-Origin >98 %, protease-free, IgG-free, nuclease-free Albumin, highly purified and tested for the absence of immunoglobulins (IgGs), proteases, RNAses, and DNAses. Albumin, IgG-free is particularly recommended for use as stabilising reagent in antibody solutions, and as blocking reagent in all assays using detection systems via antibodies. Also very well suited for stabilising of hot-start-PCRs mediated by antibodies, or as blocking reagent in antibody-detected hybridisations. Tested for the presence of proteases, IgGs, DNases and RNases.
Product Detail
For purification of this Albumin an extensive heat-shock/diafiltration method is used, which has been shown to bring more highly purified products than the standard process acc. to Cohn. The process is taking place in a closed system. Molar extinction coefficient: 4,4x10 4 L x mol -1 x cm -1 (acc. to 0,667 L x mol -1 x cm -1 for a 0,1 % solution). Bovine Serum Albumin (BSA) Fraction V, NZ-Origin >98 %, protease-free, IgG-free, nuclease-free Albumin, highly purified and tested for the absence of immunoglobulins (IgGs), proteases, RNAses, and DNAses. Albumin, IgG-free is particularly recommended for use as stabilising reagent in antibody solutions, and as blocking reagent in all assays using detection systems via antibodies. Also very well suited for stabilising of hot-start-PCRs mediated by antibodies, or as blocking reagent in antibody-detected hybridisations. Tested for the presence of proteases, IgGs, DNases and RNases.
Product Detail
ROTI ® ImmunoBlock is an innovative blocking reagent on a polymer base without detergents and proteins Suitable for: Immunocytological assays Immunohistological assays Paraffin- and cryosections in situ hybridisation Cell culture samples Whole mount samples ROTI ® ImmunoBlock 10x conc., ready-to-use The protein-free formulation prevents contamination of your detection systems by foreign proteins. Unspecific interactions of the detection reagents such as antibodies with proteins of the samples are suppressed, while the specific binding sites are retained. The signal to noise ratio is considerably increased and signal detection significantly improved. The practical ready-to-use solution makes tedious preparation unnecessary. Since the assays can be performed completely in ROTI ® ImmunoBlock, highly reproducible results are achieved. Figure: Scilla siberica : Cross section of a conducting bundle from the leaf. Immunofluorescent detection of a protein in sieve cells. a: Phase contrast; b: Immunofluorescence, blocking with ROTI ® ImmunoBlock With kind permission of Dr. Deumling, MPI for Culture Research, Cologne.
Product Detail
For purification of this Albumin an extensive heat-shock/diafiltration method is used, which has been shown to bring more highly purified products than the standard process acc. to Cohn. The process is taking place in a closed system. Molar extinction coefficient: 4,4x10 4 L x mol -1 x cm -1 (acc. to 0,667 L x mol -1 x cm -1 for a 0,1 % solution). Bovine Serum Albumin (BSA) Fraction V, NZ-Origin >98 %, protease-free, IgG-free, nuclease-free Albumin, highly purified and tested for the absence of immunoglobulins (IgGs), proteases, RNAses, and DNAses. Albumin, IgG-free is particularly recommended for use as stabilising reagent in antibody solutions, and as blocking reagent in all assays using detection systems via antibodies. Also very well suited for stabilising of hot-start-PCRs mediated by antibodies, or as blocking reagent in antibody-detected hybridisations. Tested for the presence of proteases, IgGs, DNases and RNases.
Product Detail
For purification of this Albumin an extensive heat-shock/diafiltration method is used, which has been shown to bring more highly purified products than the standard process acc. to Cohn. The process is taking place in a closed system. Molar extinction coefficient: 4,4x10 4 L x mol -1 x cm -1 (acc. to 0,667 L x mol -1 x cm -1 for a 0,1 % solution). Bovine Serum Albumin (BSA) Fraction V, NZ-Origin >98 %, protease-free, IgG-free, nuclease-free Albumin, highly purified and tested for the absence of immunoglobulins (IgGs), proteases, RNAses, and DNAses. Albumin, IgG-free is particularly recommended for use as stabilising reagent in antibody solutions, and as blocking reagent in all assays using detection systems via antibodies. Also very well suited for stabilising of hot-start-PCRs mediated by antibodies, or as blocking reagent in antibody-detected hybridisations. Tested for the presence of proteases, IgGs, DNases and RNases.
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© 2023 Copyright. All Rights Reserved. Unit 19, Euroway House, Roydsdale Way, Bradford, BD4 6SE, UK
