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EUROIMMUN cell-based assay (cba
Cell Based Assay (Cba, supplied by EUROIMMUN, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cba/cell+based+assay/nct06388161-5-2-4
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cell-based assay (cba - by Bioz Stars, 2026-09
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Article Title: Neural Autoantibody Prevalence in Patients With New-onset Focal Seizures of Unknown Etiology and a Predictive Scoring Scale
Article Snippet: Commercial cell-based assay (CBA; EUROIMMUN, Lübeck, Germany) was used to detect serum anti-N-methyl-D-aspartate receptor (anti-NMDAR), anti-α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (anti-AMPAR), anti-γ-aminobutyric acid B receptor (anti-GABABR), anti-leucine-rich glioma-inactivated 1 (anti-LGI1), anti-contactin-associated protein-like 2 (anti-CASPR2), and anti-glutamic acid decarboxylase 65 (anti-GAD65), anti-metabotropic glutamate receptor 5 (mGluR5), anti-dipeptidyl peptidase-like protein 6 (DPPX), anti-myelin oligodendrocyte glycoprotein (MOG) and anti-immunoglobulin-like cell adhesion molecule 5 (IgLON5) antibodies.

Article Title: Multifactorial analysis of clinical prognosis in patients with anti-N-methyl-D-aspartate receptor encephalitis: a single-centre cohort study.
Article Snippet: Study population and diagnostic criteria Patients were included if they met the following established diagnostic criteria for anti-NMDAR encephalitis: (i) presence of one or more of the six major symptom groups (abnormal behaviour or cognitive dysfunction, speech dysfunction, seizures, movement disorders, decreased level of consciousness and autonomic dysfunction or central hypoventilation); (ii) positive testing for NMDAR antibodies in CSF and/or serum samples using a cell-based assay (Euroimmun AG, Lübeck, Germany); and (iii) reasonable exclusion of other disorders.

Article Title: The Importance of Bright Spotty Lesions on Magnetic Resonance Imaging in Predicting Chronic Neuropathic Pain in Myelitis
Article Snippet: AQP4 IgG tests were performed using indirect immunofluorescence on a substrate of mouse cerebellum and midbrain (before 2017) and using a live-cell-based assay (EUROIMMUN, Lübeck, Germany) since 2017.

Article Title: Canine idiopathic generalized tremor syndrome, immune-mediated?
Article Snippet: When available, serum and CSF samples (stored until analysis at −80 degrees Celsius and transported on dry ice) were analyzed for neural antibodies at Laboratory Krone (Bad Salzuflen, Germany) and the analysis included a standard panel used to screen for autoantibodies against targets associated with autoimmune encephalitic diseases of humans consisting of: Cell based assay (indirect immunofluorescence (IIF), human embryonic kidney, Euroimmun, Lübeck, Germany) for antibodies against LGl1, CASPR2, NMDAR, glycine receptor (GlyR), Anti-immunoglobulin-like cell adhesion molecule 5 (IgLON5), α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPAR1/2), Gamma-amino butyric acid receptor, type B receptors (GABABR), Gamma-amino butyric acid receptor, type A receptors (GABAAR), glutamic acid decarboxylase 65-kilodalton isoform (GAD65), DPPX, metabotropic glutamate receptor 5 (mGluR5), and Metabotropic glutamate receptor 1 (mGluR1).

Article Title: Prediction model for severe autoimmune encephalitis: a tool for risk assessment and individualized treatment guidance
Article Snippet: Using the cell-based assay (CBA) method: (1) Commercial CBA kits (FA112d-1005-1, Euroimmun AG, Lübeck, Germany; MT226-16 and MT29916, Pulse Biotechnology Co., Ltd., Shaanxi, China) were utilized to detect AE antibodies in both serum and CSF of patients, including anti-N-methyl-D-aspartate receptor (NMDAR) antibody, anti- α -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR) antibody, anti-dipeptidyl-peptidase-like protein 6 (DPPX) antibody, anti-gamma-aminobutyric acid-B receptor (GABA B R) antibody, anti-leucine-rich glioma-inactivated protein 1 (LGI1) antibody, anti-contactin-associated protein-like 2 (CASPR2) antibody, anti-metabotropic glutamate receptor 5 (mGluR5) antibody, anti-IgLON5 antibody, anti-glial fibrillary acidic protein (GFAP) antibody and anti-glutamic acid decarboxylase 65 (GAD65) antibody.

Article Title: Acute neuronal cell death and neuroinflammation per se do not trigger secondary autoimmune encephalitis in mice.
Article Snippet: Autoantibody titers against 49-disease associated antibodies were determined for IgG, IgA and IgM isotypes using commercially available cell-based assays developed for the in vitro diagnostic of autoantibodies in suspected autoimmune encephalitis patients (Euroimmun biochip mosaic IVD assays).

Clinical Proteomics:

Article Title: Multifactorial analysis of clinical prognosis in patients with anti-N-methyl-D-aspartate receptor encephalitis: a single-centre cohort study.
Article Snippet: .. Anti-NMDAR antibodies were tested in both serum and CSF samples using a commercially available cellbased assay (Euroimmun AG, Lübeck, Germany), in accordance with the manufacturer’s protocol. ..



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S . Tm does not require AspC for systemic survival following intraperitoneal <t>injection.</t> <t>CBA/J</t> mice were infected with a competitive 1:1 ratio of WT and aspC -deficient S . Tm IR715 (Δ aspC ), via intraperitoneal injection at a dose of 10 4 CFU. Mice were allowed to carry the pathogen for predetermined time points prior to humane euthanasia and sample collection. ( A ) Infection schematic. ( B ) Weight-loss percentage relative to inoculation weight in mice sacrificed 3, 4, and 5 days post-infection. ( C ) Competitive index of inoculum at each time point based on the proportion of S . Tm in liver and spleen homogenates, as well as intraperitoneal lavage fluid. ( D ) S . Tm burden of each genotype in the liver. ( E ) S . Tm burden of each genotype in CFU/g in spleen. ( F ) S . Tm burden of each genotype in the intraperitoneal fluid following lavage. N = 6 per time point. Geometric mean with geometric SD. ns, not significant; ***, P < 0.001 using multiple t -test.
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S . Tm does not require AspC for systemic survival following intraperitoneal injection. CBA/J mice were infected with a competitive 1:1 ratio of WT and aspC -deficient S . Tm IR715 (Δ aspC ), via intraperitoneal injection at a dose of 10 4 CFU. Mice were allowed to carry the pathogen for predetermined time points prior to humane euthanasia and sample collection. ( A ) Infection schematic. ( B ) Weight-loss percentage relative to inoculation weight in mice sacrificed 3, 4, and 5 days post-infection. ( C ) Competitive index of inoculum at each time point based on the proportion of S . Tm in liver and spleen homogenates, as well as intraperitoneal lavage fluid. ( D ) S . Tm burden of each genotype in the liver. ( E ) S . Tm burden of each genotype in CFU/g in spleen. ( F ) S . Tm burden of each genotype in the intraperitoneal fluid following lavage. N = 6 per time point. Geometric mean with geometric SD. ns, not significant; ***, P < 0.001 using multiple t -test.

Journal: Infection and Immunity

Article Title: Aspartate aminotransferase is required for Salmonella expansion in the inflamed gut via TCA anaplerosis

doi: 10.1128/iai.00161-26

Figure Lengend Snippet: S . Tm does not require AspC for systemic survival following intraperitoneal injection. CBA/J mice were infected with a competitive 1:1 ratio of WT and aspC -deficient S . Tm IR715 (Δ aspC ), via intraperitoneal injection at a dose of 10 4 CFU. Mice were allowed to carry the pathogen for predetermined time points prior to humane euthanasia and sample collection. ( A ) Infection schematic. ( B ) Weight-loss percentage relative to inoculation weight in mice sacrificed 3, 4, and 5 days post-infection. ( C ) Competitive index of inoculum at each time point based on the proportion of S . Tm in liver and spleen homogenates, as well as intraperitoneal lavage fluid. ( D ) S . Tm burden of each genotype in the liver. ( E ) S . Tm burden of each genotype in CFU/g in spleen. ( F ) S . Tm burden of each genotype in the intraperitoneal fluid following lavage. N = 6 per time point. Geometric mean with geometric SD. ns, not significant; ***, P < 0.001 using multiple t -test.

Article Snippet: Seven-week-old CBA/J mice were purchased from Jackson Labs Inc., infected with 10 4 CFU of each strain, and carried for 96 h post-infection before sacrifice.

Techniques: Injection, Infection

Deletion of aspC results in a significant expansion defect only in the cecum and colon during a murine model of gastroenteritis. To interrogate the necessity of AspC via the canonical fecal-oral route of infection, we gavaged CBA/J mice with a 1:1 competitive ratio of our WT S . Tm and isogenic Δ aspC mutant. ( A ) Schematic for competitive in vivo infection. ( B ) Competition index of inoculum over time in feces. ( C and D ) Competition index of inoculum 10 d.p.i. from systemic and gut lumen samples of infected mice. To corroborate our observations, we repeated our infection with either of our strains in isolation. ( E ) Schematic for single infection. ( F ) S . Tm burden in feces over time in mice infected with either WT S . Tm or Δ aspC mutant. N = 6 per condition. Geometric mean and geometric SD. *, P < 0.05; **, P < 0.01 using Mann-Whitney ( B ), paired-end ( E ), or unpaired t -test ( F ).

Journal: Infection and Immunity

Article Title: Aspartate aminotransferase is required for Salmonella expansion in the inflamed gut via TCA anaplerosis

doi: 10.1128/iai.00161-26

Figure Lengend Snippet: Deletion of aspC results in a significant expansion defect only in the cecum and colon during a murine model of gastroenteritis. To interrogate the necessity of AspC via the canonical fecal-oral route of infection, we gavaged CBA/J mice with a 1:1 competitive ratio of our WT S . Tm and isogenic Δ aspC mutant. ( A ) Schematic for competitive in vivo infection. ( B ) Competition index of inoculum over time in feces. ( C and D ) Competition index of inoculum 10 d.p.i. from systemic and gut lumen samples of infected mice. To corroborate our observations, we repeated our infection with either of our strains in isolation. ( E ) Schematic for single infection. ( F ) S . Tm burden in feces over time in mice infected with either WT S . Tm or Δ aspC mutant. N = 6 per condition. Geometric mean and geometric SD. *, P < 0.05; **, P < 0.01 using Mann-Whitney ( B ), paired-end ( E ), or unpaired t -test ( F ).

Article Snippet: Seven-week-old CBA/J mice were purchased from Jackson Labs Inc., infected with 10 4 CFU of each strain, and carried for 96 h post-infection before sacrifice.

Techniques: Infection, Mutagenesis, In Vivo, Isolation, MANN-WHITNEY

Genetic inactivation of T3SSs results in a colonization defect of Δ aspC but does not alter the overall expansion defect. We constructed isogenic S . Tm Δ aspC mutants in an avirulent background (Δ invA Δ spiB ) and repeated the competitive infection experiment in CBA/J mice, comparing the avirulent strains to the S . Tm WT background. ( A ) Infection schematic of competitive infection. ( B ) Competitive index of inoculum in feces over the course of the infection. Day 3 samples were not collected. ( C and D ) Competitive index of inoculum ( C ) and CFU counts ( D ) of S . Tm strains in cecal content at 10 d.p.i. ( E and F ) Competitive index of inoculum ( E ) and CFU counts ( F ) of S . Tm strains in colon content at 10 d.p.i. N = 6. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001 using unpaired ( B ) or paired t -test ( E, F ).

Journal: Infection and Immunity

Article Title: Aspartate aminotransferase is required for Salmonella expansion in the inflamed gut via TCA anaplerosis

doi: 10.1128/iai.00161-26

Figure Lengend Snippet: Genetic inactivation of T3SSs results in a colonization defect of Δ aspC but does not alter the overall expansion defect. We constructed isogenic S . Tm Δ aspC mutants in an avirulent background (Δ invA Δ spiB ) and repeated the competitive infection experiment in CBA/J mice, comparing the avirulent strains to the S . Tm WT background. ( A ) Infection schematic of competitive infection. ( B ) Competitive index of inoculum in feces over the course of the infection. Day 3 samples were not collected. ( C and D ) Competitive index of inoculum ( C ) and CFU counts ( D ) of S . Tm strains in cecal content at 10 d.p.i. ( E and F ) Competitive index of inoculum ( E ) and CFU counts ( F ) of S . Tm strains in colon content at 10 d.p.i. N = 6. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001 using unpaired ( B ) or paired t -test ( E, F ).

Article Snippet: Seven-week-old CBA/J mice were purchased from Jackson Labs Inc., infected with 10 4 CFU of each strain, and carried for 96 h post-infection before sacrifice.

Techniques: Construct, Infection