Search results for: Anti-human Apolipoprotein-H (β2-Glycoprotein-I ) Antibody
#34283639 2021/07/19 To Up
Epitope Mapping of an Antihuman EGFR Monoclonal Antibody (EMab-134) Using the REMAP Method.The epidermal growth factor receptor (EGFR) is a tyrosine kinase receptor that plays an important role in normal epidermal cell physiology. EGFR is overexpressed in cancer cells and has a number of mutations that implicate tumor malignancy, development, and poor patient prognosis; thus, EGFR is an attractive target for cancer therapy. At present, anti-EGFR monoclonal antibodies (mAbs) have been approved and are used for treating patients with a variety of EGFR-expressing cancers. Epitope mapping is important in identifying the therapeutic mechanism of anti-EGFR mAbs; however, the development of epitope mapping techniques lags behind the development of antimolecular target mAbs, including anti-EGFR mAbs. Hence, in this study, a novel epitope mapping method, RIEDL insertion for epitope mapping (REMAP) method, was developed. The results of this study demonstrated that the critical epitope of anti-EGFR mAb EMab-134 is Gly378, Asp379, Ser380, Phe381, Thr382, His383, Thr384, Pro385, and Pro386 of EGFR. The REMAP method could be useful for determining the critical epitope of functional mAbs against many target molecules.
Masato Sano, Mika K Kaneko, Teizo Aasano, Yukinari Kato
2988 related Products with: Epitope Mapping of an Antihuman EGFR Monoclonal Antibody (EMab-134) Using the REMAP Method.100ug Lyophilized100 μg100ul100 ug1 mg100ug Lyophilized0.25 mg100 ug0.1 mg50 ug
#34173367 2021/06/22 To Up
Filaggrin Expression in the Lid Margin During Contact Lens Wear.To investigate the expression of the keratinization-related protein, filaggrin, in the lid margin epithelium of contact lens (CL) wearers compared with nonwearers.
Waleed M Alghamdi, Maria Markoulli, Eric B Papas300 units1100 units
#34170640 // To Up
Anti-ALe: a mind boggler.The Lewis blood group system is unique because antigens are neither alleles of the same gene nor are they synthesized by red blood cells (RBCs); rather, they are adsorbed onto the RBC membrane from plasma as glycolipids. Antibodies against Lewis antigens are predominantly naturally occurring immunoglobulin (Ig)M type that sometimes react at 37Â°C and the antihuman globulin phase. Lewis compound antigens, ALe and BLe, have been described that were confirmed because of the presence of antibodies against them. These compound antigens are the result of an interaction between , and genes.
A Gupta, K Chaudhary, S Asati, B Kakkar100ug Lyophilized100ug Lyophilized100 Tests0.1 mg413 μg100ug100ug Lyophilized100 μg100μl100ug500 100
#34150714 2021/06/02 To Up
Oriented Antibody Covalent Immobilization for Label-Free Impedimetric Detection of C-Reactive Protein Direct and Sandwich Immunoassays.The detection and monitoring of biological markers as disease indicators in a simple manner is a subject of international interest. In this work, we report two simple and sensitive label-free impedimetric immunoassays for the detection of C-reactive protein (CRP). The gold electrode modified with boronic acid-terminated self-assembled monolayers afforded oriented immobilization of capture glycosylated antibody (antihuman CRP monoclonal antibody, mAb). This antibody-modified surface was able to capture human CRP protein, and the impedance signal showed linear dependence with CRP concentration. We confirmed the immobilization of anti-CRP mAb using surface sensitive X-ray photoelectron spectroscopy (XPS) and electrochemical impedance. The oriented covalent immobilization of mAb was achieved using glycosylated Fc (fragment, crystallizable) region specific to boronic acid. The direct immunoassay exhibited a linear curve for concentration range up to 100Â ngÂ ml. The limit of detection (LoD) of 2.9Â ngÂ ml, limit of quantification (LoQ) of 9.66Â ngÂ ml, and sensitivity of 0.585Â kÎ©Â ngÂ mlÂ cm were obtained. The sandwich immunoassay was carried out by capturing polyclonal anti-CRP antibody (pAb) onto the CRP antigen immunoreaction. The impedance signal after pAb capture also showed linear dependence with CRP antigen concentration and acted as a CRP antigen detection signal amplifier. The detection of the CRP antigen using sandwich pAb immunoassay improved LoD to 1.2Â ngÂ ml, LoQ to 3.97Â ngÂ ml, and enhanced the sensitivity to 0.885Â kÎ©Â ngÂ mlÂ cm. The real sample analysis, using newborn calf serum, showed excellent selectivity and % recovery for the human CRP ranging from 91.2 to 96.5%. The method was reproducible to 4.5% for direct immunoassay and 2.3% for sandwich immunoassay.
Abiola Adesina, Philani Mashazi
1029 related Products with: Oriented Antibody Covalent Immobilization for Label-Free Impedimetric Detection of C-Reactive Protein Direct and Sandwich Immunoassays.20 ml1 mg1mg2 mg 200ul100 ul1 mg1mg100ul1 mg100
#34028385 2021/05/19 To Up
Stability of Antihuman Leukocyte Antigen Sensitization Profiles in Highly Sensitized Kidney Transplantation Candidates: Towards a Rational Serological Testing Strategy.Highly sensitized (HS) anti-human leukocyte antigens (HLA) patients awaiting kidney transplantation benefit from specific allocation programs. Serological monitoring at 3-month intervals is recommended to prevent unexpected positive crossmatch (XM), but this strategy is not evidence-based. Therefore, we assessed its relevance when using single-antigen flow bead (SAFB) and screening flow bead (SFB) assays.
Elodie Wojciechowski, FrÃ©dÃ©ric Jambon, Marine Cargou, Gwendaline Guidicelli, Pierre Merville, Lionel Couzi, Jean-Luc Taupin, Jonathan Visentin
2073 related Products with: Stability of Antihuman Leukocyte Antigen Sensitization Profiles in Highly Sensitized Kidney Transplantation Candidates: Towards a Rational Serological Testing Strategy.4 Arrays/Slide2 Pieces/Box4 Membranes/Box2 Pieces/Box4 Membranes/Box2 Pieces/Box0.1ml4 Arrays/Slide
#33967482 2021/01/09 To Up
Immunohistochemical analysis of Nuclear Factor-kappa B (NF-ÎºB) between follicular and plexiform ameloblastomas: A pilot study.Ameloblastoma among benign tumors holds a unique position by its locally destructive and invasive nature. Tumors that originate from the odontogenic apparatus or its remnants in the jaws show diverse clinical presentations, behavior and histologic patterns. The differed biological behavior behind follicular and plexiform ameloblastomas has never attained completeness because of the lack of rhythmic correlation regarding the exact mechanism. Nuclear factor-kappa B (NF-ÎºB) pathways play a crucial role in survival, death and differentiation during physiologic and pathologic conditions. With this background, the study has been aimed to investigate the expression of NF-ÎºB in follicular and plexiform ameloblastomas.
Muniapillai Sivakumar, Thuckanaickenpalayam Ragunathan Yoithapprabhunath, Ramadas Madhavan Nirmal, Veeran Veeravarmal, Janardhanam Dineshshankar, Ramamoorthy Amsaveni
1701 related Products with: Immunohistochemical analysis of Nuclear Factor-kappa B (NF-ÎºB) between follicular and plexiform ameloblastomas: A pilot study.1 mg100ug100ug10mg 100ul100ug Lyophilized100.00 ug1 mg1.0 mg1 mg 120 ml
#33967093 // To Up
A case of HIV negative cryptococcal meningitis with antiphospholipid syndrome.Cryptococcal meningitis has become the largest cause for the death of infectious diseases in the central nervous system infectious disease worldwide. Most patients with cryptococcal meningitis have AIDS, autoimmune diseases, hematologic malignancies, and some other relevant diseases. It is mainly caused by infection with or . Although the relationship between cryptococcal meningitis and autoimmune diseases, such as systemic lupus erythematosus, has been recognized, little has been studied about it. Furthermore, with the use of glucocorticoids and immunosuppressants, the incidence of cryptococcal meningitis is increasing year by year. Cryptococcal meningitis accounts for 15% of HIV-related deaths globally, compared with little research on HIV-negative cryptococcal diseases. A 54-year-old female patient with gingival bleeding was admitted to the Department of Neurology at the Second Xiangya Hospital of Central South University. The patient subsequently developed a series of central nervous system symptoms such as headache, ischemic stroke, and epilepsy. The number of thrombocytes was at 4Ã10/L, antinuclear antibody was (+), antihuman globulin was (++), globulin IgG anticardiolipin antibody IgG, IgA, and IgM was positive, lupus anticoagulant was strong positive, antibody against Î²2 glycoprotein 1 IgM >841 AU/mL with elevated cerebrospinal fluid (CSF) pressure. The CSF India ink staining was positive, CSF was cultured cryptococcus neoformans. Antiphospholipid syndrome (APS) and cryptococcal neoformans meningitis were diagnosed. After active antifungal therapy and control of APS, the patient still had a serial of complications including high CSF pressure, persistent positive India ink staining, refractory electrolyte disturbance, hemolytic anemia recurs, heart failure, and finally death. No cases of the combination of the two diseases have been reported, and this case of cryptococcal meningitis with APS may provide a new direction to the diagnosis and treatment for this kind of disease.
Jing Zhao, Xiaomei Wu, Zhonghua Huang, Jie Zhang
2939 related Products with: A case of HIV negative cryptococcal meningitis with antiphospholipid syndrome.0.1ml
#33962486 // To Up
Comparative evaluation of the conventional tube test and column agglutination technology for ABO antibody titration in healthy individuals: a report from India.Determination of accurate anti-A/-B titers is important for treatment selection in ABO-incompatible stem cell and solid-organ transplants. The standard method for ABO antibody titration is the conventional tube test (CTT). Dithiothreitol (DTT) is commonly used to inactivate the IgM antibody component. The aim of this study was to compare six different methods for ABO antibody titration and to observe the effectiveness of DTT on antibody estimation. A total of 90 healthy voluntary blood donors were enrolled in this study, including 30 each for blood groups A, B, and O. Antibody titrations were performed and tested using the CTT-immediate spin (IS), CTT-antihuman globulin (AHG) with and without DTT, column agglutination technology (CAT)-IS, and CAT-AHG with and without DTT methods. Bead-CAT was used, and the positive cutoff value was set to 1+ for each method to determine the endpoint of the titer. The median values of anti-A/-B titers by IS were found to be higher than those values by AHG in CTT and CAT among group B and A individuals, whereas no statistically significant differences were observed in values from group O individuals for IS and AHG anti-A/-B titers, estimated by each method. Although there was positive correlation between the anti-A/-B titer results obtained using the CTT and CAT in all blood groups, testing using AHG showed poor agreement with and without DTT pretreatment (kappa value of 0.11 and 0.20, respectively). Moderate agreement was observed between CTT-IS and CAT-IS (kappa value of 0.46). Median anti-A/-B AHG titers were reduced by the use of DTT in all blood group samples. Significant differences in the interpretability of anti-A/-B titers were observed among different methods. A uniform approach for selecting the method for ABO antibody titration is highly recommended, and DTT pretreatment of plasma to neutralize IgM activity should be considered to obtain precise values of IgG anti-A/-B titers. .
S S Datta, S Basu, M Reddy, K Gupta, S Sinha
1648 related Products with: Comparative evaluation of the conventional tube test and column agglutination technology for ABO antibody titration in healthy individuals: a report from India.100 TESTS1,000 tests1000 tests1000 tests500 tests500 tests
#33920860 2021/04/15 To Up
Characterization of Dog Glutathione Transferase P1-1, an Enzyme Relevant to Veterinary Medicine.Glutathione transferases (GSTs) form a family of detoxication enzymes instrumental in the inactivation and elimination of electrophilic mutagenic and carcinogenic compounds. The Pi class GST P1-1 is present in most tissues and is commonly overexpressed in neoplastic cells. GST P1-1 in the dog, , has merits as a marker for tumors and as a target for enzyme-activated prodrugs. We produced the canine enzyme CluGST P1-1 by heterologous bacterial expression and verified its cross-reactivity with antihuman-GST P1-1 antibodies. The catalytic activity with alternative substrates of biological significance was determined, and the most active substrate found was benzyl isothiocyanate. Among established GST inhibitors, Cibacron Blue showed positive cooperativity with an IC value of 43 nM. Dog GST P1-1 catalyzes activation of the prodrug Telcyta, but the activity is significantly lower than that of the human homolog.
Aram Ismail, Elizabeth Lewis, Birgitta SjÃ¶din, Bengt Mannervik
1157 related Products with: Characterization of Dog Glutathione Transferase P1-1, an Enzyme Relevant to Veterinary Medicine.100ul 100ul1 mg500 0.1ml (1mg/ml)200 1 mL1 module100μg100ug/vial100 ul100 μg
#33900821 // To Up
Suppression of Th1 and Th17 Proinflammatory Cytokines and Upregulation of FOXP3 Expression by a Humanized Anti-DNAM-1 Monoclonal Antibody.DNAM-1 is an activating immunoreceptor expressed on hematopoietic cells, including both CD4 and CD8 T cells, natural killer cells, and platelets. Since DNAM-1 is involved in the pathogenesis of various inflammatory diseases and cancers in humans as well as mouse models, it is a potential target for immunotherapy for these diseases. In this study, we generated a humanized neutralizing antihuman DNAM-1 monoclonal antibody (mAb), named TNAX101A, which contains an engineered Fc portion of human IgG1 to reduce Fc-mediated effector functions. We show that TNAX101A efficiently interfered the binding of DNAM-1 to its ligand CD155 and showed unique functions; it decreased production of the inflammatory cytokines such as interferon-gamma, tumor necrosis factor alpha, interleukin (IL)-6, IL-17A, and IL-17F by anti-CD3 antibody-stimulated or alloantigen-stimulated T cells and increased FOXP3 expression in anti-CD3-stimulated regulatory T (Treg) cells. These dual functions of TNAX101A may be advantageous for the treatment of T cell-mediated inflammatory diseases through both downregulation of effector T cell function and upregulation of Treg cell function.
Yumi Yamashita-Kanemaru, Kyoko Oh-Oka, Fumie Abe, Kazuko Shibuya, Akira Shibuya
1968 related Products with: Suppression of Th1 and Th17 Proinflammatory Cytokines and Upregulation of FOXP3 Expression by a Humanized Anti-DNAM-1 Monoclonal Antibody.100ul100ug100ul100ul100ug100ul100ul100ul100ug Lyophilized100μl100ul100ul
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