Antibodies Assay Kits Bap1 Antibody Biology Cells Brd4 Antibody Canine Albumin cDNA Gels Glut2 Antibody Gsk3 Alpha Laminin Alpha 5 Nedd4 Antibody Nox1 Antibody Nse Antibody Panel Particles PCR Pcr Kits Peptides Pkr Antibody Secreted Alkaline Phosphatase Stat5 Antibody Tcf4 Antibody Test Kits Tgf Alpha Antibody Tgf Alpha Elisa
Nanometer-Sized Boron Loaded Liposomes Containing Fe 3 O 4 Magnetic Nanoparticles and Tributyl Borate and Anti-Albumin from Bovine Serum Antibody for Thermal Neutron Detection
A scarcity within the provide of 3He used for thermal neutron detector makes researchers to seek out 3He options for creating new neutron detectors. Right here, we ready a neutron-sensitive composite liposome with tributyl borate and encapsulating with Fe3O4@oleic acid nanoparticles (Fe3O4@OA NPs), methylene blue (MB), or anti-albumin from bovine serum (anti-BSA).
The tributyl borate compound was characterised by Fourier remodel infrared spectroscopy (FT-IR). As well as, the morphology, aspect compositions, and magnetic properties of the composite liposome had been investigated with transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), and vibrating pattern magnetometer (VSM), respectively.
The outcomes indicated {that a} typical ellipsoidal magnetic liposome construction was obtained, and the lengths of the minor axis and main axis had been 49 ± 1 nm and 87 ± Three nm, respectively. Beneath thermal neutron irradiation, the construction of composite liposome was destroyed, and encapsulated reporter molecules had been launched, which was detected by ultraviolet-visible (UV-vis) spectroscopy and floor plasmon resonance (SPR) know-how.
The response of this sensor based mostly on a damaging assay exhibits a superb correlation with neutron doses. Apart from, the sensor has a neutron to gamma-ray rejection ratio of 1568 at a thermal neutron flux charge of 135.6 n/cm2·s, which makes it a promising different to 3He.
Detection of Six β-Agonists by Three Multiresidue Immunosensors Based mostly on an Anti–bovine Serum Albumin-Ractopamine-Clenbuterol-Salbutamol Antibody.
In keeping with an oblique aggressive immunoassay, six β-agonists (clenbuterol (CL), salbutamol (SAL), ractopamine (RAC), terbutaline (TER), mabuterol (MAB), and tulobuterol (TUL)) had been detected by three novel multiresidue immunosensors on the premise of the profitable preparation of bovine serum albumin (BSA)-RAC-CL-SAL multideterminant antigen and anti-BSA-RAC-CL-SAL antibody.
A brand new technique was reported to detect six β-agonists by combining nanotechnology, electrochemical detection, and particular immune know-how. On the similar focus, the amperometric response for detection of six β-agonists was in a sequence of GCE/GNP/SAL > GCE/GNP/RAC > GCE/GNP/CL. Detection limits of six β-agonists present that the multiresidue detection efficiency of the GCE/GNP/RAC immunosensor is healthier than these of GCE/GNP/SAL and GCE/GNP/CL immunosensors.
Three immunosensors manifest superior properties with a large linear vary, low detection restrict, wonderful reproducibility, and stability. The proposed GCE/GNP/RAC immunosensor shows excessive accuracy and may be successfully used for actual pattern detection.
Investigation of the antigen antibody response between anti–bovine serum albumin (a-BSA) and bovine serum albumin (BSA) utilizing piezoresistive microcantilever based mostly sensors.
A brand new microsensor utility based mostly on piezoresistive microcantilever know-how has been used to review the interplay of anti-bovine serum albumin (a-BSA) with bovine serum albumin (BSA). A skinny layer of BSA hooked up to a glass slide was used because the lively sensing layer for the detection of a-BSA in resolution. This design produced a big, constant cantilever deflection when uncovered to the analyte.
On this system, the cantilever deflection is measured as a easy resistance change within the piezoresistive channel throughout the cantilever. In a second set of experiments, 3:1 BSA:PEO protein/polymer blended substrates had been used because the lively sensing layer for the detection of a-BSA in an aerosol supply. A definite signature for the analyte, separate from the water vapor provider, is obtained for this technique.
ABP(57) is an auxin-binding protein that possesses receptor operate. On this examine, a protocol for ABP(57) purification was developed on the premise of cross-reactivity proven between ABP(57) and antisera raised in opposition to bovine serum albumin, which enabled us to purify ABP(57) with a excessive yield and to additional characterize it. ABP(57) prompts plant plasma membrane H(+)-ATPase (PM H(+)-ATPase) by way of direct interplay.
The binding of indole-3-acetic acid (IAA) to the first binding website on ABP(57) triggered a marked enhance within the affinity of ABP(57) for PM H(+)-ATPase, which was accompanied by a change in ABP(57) conformation. In the meantime, further IAA binding to the secondary website on ABP(57) nullified the preliminary impact with out inducing additional conformational change.
When ABP(57) with IAA occupying solely the first website interacted with PM H(+)-ATPase, no IAA may entry the secondary website. These outcomes counsel that IAA-induced biphasic alteration within the affinity of ABP(57) for PM H(+)-ATPase correlates with a bell-shaped dose response of the enzyme to IAA. There’s additionally a chance that, whereas the stimulation part of the response is related to a conformational change of ABP(57), the destimulation part most likely outcomes from hindrance arising instantly from the presence of IAA on the secondary website.
Polyclonal rabbit anti-idiotypic (Ab2) antibodies raised in opposition to the antiprogesterone mAb DB3 (Ab1) had been used to induce an Ab3 antiprogesterone response in BALB/c mice. Whereas the affinity of Ab3 sera for progesterone was 10-50-times decrease than that of DB3, their steroid-binding specificity confirmed appreciable similarity to DB3.
Two immunoglobulin M (IgM) Ab3 monoclonal antibodies (mAbs), 1A4 and 3B11, had been obtained, each of which sure progesterone conjugated to bovine serum albumin (progesterone-BSA). 1A4 additionally sure free progesterone, though with low affinity and really broad cross-reactivity. Like DB3, 1A4 is encoded by a heavy-chain variable area (VH) gene section from the small VGAM3.eight household, a restriction that’s attribute of antibodies raised in opposition to progesterone-11alpha-BSA.
In distinction, 3B11 binds progesterone-11alpha-BSA however not free progesterone and is encoded by an unrelated VH gene from the J558 household. The sunshine chain variable area (VL) of 1A4 lacks the intradomain disulphide bridge owing to substitute of CysL23 by Tyr.
Bovine Serum Albumin Antibody |
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| MBS8584301-01mLAF405L | MyBiosource | 0.1mL(AF405L) | EUR 465 |
Bovine Serum Albumin Antibody |
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| MBS8584301-01mLAF405S | MyBiosource | 0.1mL(AF405S) | EUR 465 |
Bovine Serum Albumin Antibody |
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| MBS8584301-01mLAF610 | MyBiosource | 0.1mL(AF610) | EUR 465 |
Bovine Serum Albumin Antibody |
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| MBS8584301-01mLAF635 | MyBiosource | 0.1mL(AF635) | EUR 465 |
Bovine Serum Albumin Antibody |
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| C42100-100ul | Assay Biotech | 100μl | EUR 217 |
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Description: Bovine Serum Albumin Rabbit Polyclonal Antibody |
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Bovine Serum Albumin Antibody |
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| C42100-50ul | Assay Biotech | 50μl | EUR 143.5 |
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Description: Bovine Serum Albumin Rabbit Polyclonal Antibody |
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Bovine Serum Albumin Antibody (HRP) |
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| 20-abx134735 | Abbexa |
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Bovine Serum Albumin Antibody (HRP) |
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| GWB-9ED714 | GenWay Biotech | 1 mg | Ask for price |
Bovine Serum Albumin Antibody / BSA |
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| V3048-100UG | NSJ Bioreagents | 100 ug | EUR 424.15 |
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Description: Reacts with a protein of ~66kDa, identified as bovine serum albumin (BSA). It is a high affinity antibody and can be used for detection of traces of BSA. Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. BSA makes up about half of the protein in plasma and represents the most stable and soluble protein in the plasma. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. The BSA component contains several lysines that are capable of reacting with conjugation sites of linkers, making it applicable as a carrier protein for antigenic compounds. |
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Bovine Serum Albumin Antibody / BSA |
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| V3048-20UG | NSJ Bioreagents | 20 ug | EUR 186.15 |
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Description: Reacts with a protein of ~66kDa, identified as bovine serum albumin (BSA). It is a high affinity antibody and can be used for detection of traces of BSA. Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. BSA makes up about half of the protein in plasma and represents the most stable and soluble protein in the plasma. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. The BSA component contains several lysines that are capable of reacting with conjugation sites of linkers, making it applicable as a carrier protein for antigenic compounds. |
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Bovine Serum Albumin Antibody / BSA |
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| V3048SAF-100UG | NSJ Bioreagents | 100 ug | EUR 424.15 |
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Description: Reacts with a protein of ~66kDa, identified as bovine serum albumin (BSA). It is a high affinity antibody and can be used for detection of traces of BSA. Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. BSA makes up about half of the protein in plasma and represents the most stable and soluble protein in the plasma. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. The BSA component contains several lysines that are capable of reacting with conjugation sites of linkers, making it applicable as a carrier protein for antigenic compounds. |
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Bovine Serum Albumin Antibody / BSA |
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| V3049-100UG | NSJ Bioreagents | 100 ug | EUR 424.15 |
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Description: Reacts with a protein of ~66kDa, identified as bovine serum albumin (BSA). It is a high affinity antibody and can be used for detection of traces of BSA. Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. BSA makes up about half of the protein in plasma and represents the most stable and soluble protein in the plasma. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. The BSA component contains several lysines that are capable of reacting with conjugation sites of linkers, making it applicable as a carrier protein for antigenic compounds. |
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Bovine Serum Albumin Antibody / BSA |
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| V3049-20UG | NSJ Bioreagents | 20 ug | EUR 186.15 |
|
Description: Reacts with a protein of ~66kDa, identified as bovine serum albumin (BSA). It is a high affinity antibody and can be used for detection of traces of BSA. Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. BSA makes up about half of the protein in plasma and represents the most stable and soluble protein in the plasma. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. The BSA component contains several lysines that are capable of reacting with conjugation sites of linkers, making it applicable as a carrier protein for antigenic compounds. |
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Bovine Serum Albumin Antibody / BSA |
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| V3049SAF-100UG | NSJ Bioreagents | 100 ug | EUR 424.15 |
|
Description: Reacts with a protein of ~66kDa, identified as bovine serum albumin (BSA). It is a high affinity antibody and can be used for detection of traces of BSA. Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. BSA makes up about half of the protein in plasma and represents the most stable and soluble protein in the plasma. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. The BSA component contains several lysines that are capable of reacting with conjugation sites of linkers, making it applicable as a carrier protein for antigenic compounds. |
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Bovine Serum Albumin Antibody / BSA |
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| V7183-100UG | NSJ Bioreagents | 100 ug | EUR 424.15 |
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Description: Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. |
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Bovine Serum Albumin Antibody / BSA |
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| V7183-20UG | NSJ Bioreagents | 20 ug | EUR 186.15 |
|
Description: Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. |
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Bovine Serum Albumin Antibody / BSA |
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| V7183SAF-100UG | NSJ Bioreagents | 100 ug | EUR 424.15 |
|
Description: Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. |
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Bovine Serum Albumin Antibody (FITC) |
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| 20-abx134738 | Abbexa |
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Each the 1A4 and 3B11 heavy chains have extraordinarily brief complementarity figuring out area (CDR) H3 loops, comprising three and 4 amino acids, respectively. Modelling of the combining website of 1A4 from the X-ray crystallographic construction of DB3 signifies that the brief H3 loop is a significant factor within the lack of affinity and specificity for steroid.
