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Globulins

Globulins are a class of proteins found in the blood plasma and other bodily fluids.
They play a crucial role in the immune system, serving as antibodies and other important biological functions.
Globulins can be further classified into different subtypes, such as alpha, beta, and gamna globulins, each with their own specific functions and characteristics.
Researchers can utlize PubCompare.ai's AI-powered platform to optimize their globulin studies, easily locating relevant protocols and identifying the best products and methods to drive their research forward and ensure reproducibility.

Most cited protocols related to «Globulins»

The study included 201 consecutive patients with liver cirrhosis admitted to two Liver Units of university/primary hospitals in Southern Italy, between the period from October 2004 to June 2007 who fulfilled the following criteria: patients' willingness to undergo previously established screening; endoscopic, US and laboratory examinations performed within four weeks of each other; prospective follow-up for a minimum period of 6 months.
Of initial patients, 26 were kept out because their US and laboratory examinations had been previously performed in different centres. Fourteen patients, who had undergone endoscopic esophageal variceal ligation therapy, and eight who had received beta-blockers before US imaging, were also excluded from the study because prior treatment might have caused a change in lesion features.
The remaining 153 patients formed the study population (85 males) whose age ranged from 31 to 85 years (median age 66 years). Chronic liver damage in these patients was caused by hepatitis B (n = 9), hepatitis C (n = 114), alcohol abuse (n = 20) or unknown etiology, likely NonAlcoholic Steato Hepatitis (NASH), (n = 8). Ninety two patients had compensated cirrhosis of the liver. For 121 patients, the diagnosis of cirrhosis was established by contextual clinical (spider nevi, organomegaly) laboratory (low total cholesterol and pseudocholinesterase levels, reduced white blood cell count, globulin/albumin ratio > 1), antecedent imaging data and for 32 patients by biopsy. The non-invasive assessment of liver cirrhosis was blindly performed de novo to all patients by radiologists on the basis of US/US-doppler examinations (coarse echo-texture, nodularity presence, increased caudate/right lobe ratio, hypertrophy of the left lobe, characterized by a rounded inferior marginal edge, and portal vein enlargement with decreased flow velocity, absence of a normal doppler waveform, hepatofugal flow). No evidence of hepatocellular carcinoma at the first hepatic decompensation was detected. Renal insufficiency was properly excluded.
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Publication 2009
Abuse, Alcohol Adrenergic beta-Antagonists Albumins Biopsy Butyrylcholinesterase Cholesterol Diagnosis ECHO protocol Endoscopy Globulins Hepatitis Hepatitis B Hepatitis C virus Hepatocellular Carcinomas Hypertrophy Leukocyte Count Ligation Liver Liver Cirrhosis Males Nevus Patients Physical Examination Radiologist Renal Insufficiency Spiders Ultrasounds, Doppler Veins Veins, Portal
Human serum albumin (fatty acid and globulin free, ≥99% pure), phenylbutazone, and 5-dimethylamino-1-naphthalenesulfonamide (dansylamide; DNSA) were purchased from Sigma-Aldrich (St. Louis, MO). Flufenamic acid was purchased from Fluka Analytical (Buchs, Switzerland), and dansyl-L-proline (DP) was purchased from TCI (Cambridge, MA). The synthesis and characterization of 4 OH PCB 52 (2,2’,5,5’-tetrachlorobiphenyl-4-ol) and 4 PCB 52 sulfate (sulfuric acid mono-(2,2’,5,5’-tetrachlorobiphenyl-4-yl) ester, ammonium salt) are reported in the Supporting Information. All other PCB metabolites were prepared and characterized in the synthesis core of the Iowa Superfund Research Program as previously described.43 (link)–45 (link)
Publication 2016
5-dimethylaminonaphthalene-1-sulfonamide Anabolism Chloride, Ammonium dansylproline Esters Fatty Acids Flufenamic Acid Globulins naphthalenesulfonamide PCB 52 Phenylbutazone Serum Albumin, Human Sulfates, Inorganic Sulfuric Acids
Defatted flours (2 × 50 g) were extracted three times each with 200 mL of (a) salt solution by homogenizing with an Ultra Turrax blender (16 000 rpm, IKA-Werke, Staufen, Germany) in a centrifuge vessel for 5 min at 22°C. The suspensions were centrifuged (3750 × g, 25 min, 22°C) and the supernatants discarded (→ ALGL fraction). The sediments were extracted three times with 200 mL of (b) ethanol/water as described for the ALGL fraction. The resulting supernatants were combined, concentrated under reduced pressure, dialyzed (Mr cut-off: 12 000–14 000, Medicell Membranes, London, UK) and lyophilized (→ prolamin fraction). Then, the sediments were extracted three times under nitrogen with 200 mL of (c) glutelin solution (see above) by homogenizing with an Ultra Turrax blender for 5 min, stirring for 30 min at 60°C, cooling and centrifugation as described. The supernatants were combined, concentrated, dialyzed and lyophilized (→ glutelin fraction). For oat flour, the extraction was stopped after the prolamin fraction (Mr cut-off for dialysis: 7 000, Medicell Membranes), because oat glutelins are mainly composed of polymeric 12S globulins [30 ]. The CP contents of the dried prolamin and glutelin fractions were determined according to ICC Standard 167 (n = 3) [24 ].
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Publication 2017
Blood Vessel Centrifugation Dialysis Ethanol Flour Globulins Glutelins Nitrogen Polymers Pressure Prolamins Sodium Chloride Tissue, Membrane Wheat Flour
Methods for study of rat adrenal function were adapted and optimized from several previously published reports.26 (link)–28 (link) Immediately following weighing and IV catheter placement, dexamethasone (0.2 mg/kg IV; American Regent, Shirley, NY) was administered to each rat to inhibit endogenous adrenocorticotropic hormone (ACTH) release, to suppress baseline corticosterone production, and to inhibit the variable stress response to restraint and handling. The IV tail vein catheter, used for both drug administration and blood draws, was heparin-locked after each use with 10 U/ml heparin to maintain patency; the heparin locking solution was “wicked” out of the catheter prior to drug administration and blood draws to minimize rat and sample heparinization. All blood draws were approximately 0.3 mls in volume. All drugs administrations were followed by a 1 ml normal saline flush to assure complete drug delivery.
Two hours following dexamethasone treatment, blood was drawn (for baseline measurement of serum corticosterone concentration) and a second dose of dexamethasome (0.2 mg/kg) was administered along with either IV MOC-etomidate, etomidate, propofol, or vehicle (35% propylene glycol v/v in water) as a control. Fifteen minutes later, ACTH1–24 (25 μg/kg; Sigma-Aldrich Chemical Co, St. Louis, MO) was given intravenously to stimulate corticosterone production. Fifteen minutes after ACTH1–24 administration (i.e., 30 min after drug or vehicle administration), a second blood sample was drawn to measure the ACTH1–24-stimulated serum corticosterone concentration. ACTH1–24 was dissolved in 1 mg/ml in deoxygenated water as stock, aliquoted, and frozen (−20 °C); a fresh aliquot was thawed just prior to each use. Rats in all three groups (vehicle, etomidate, and MOC-etomidate) received the same volume of propylene glycol.
Blood samples were allowed to clot at room temperature (10 to 60 min) before centrifugation at 3500g for 5 min. Serum was carefully expressed from any resulting superficial fibrin clot using a clean pipette tip prior to a second centrifugation at 3500g for 5 min. Following the second centrifugation, the resultant straw colored, clot-free serum layer was transferred to a fresh vial for a final, high-speed centrifugation (16000g, for 5 min) to pellet any contaminating red blood cells or particulates. The serum was transferred to a clean vial and promptly frozen (−20 °C) pending corticosterone measurement within 1 to 2 days. Following thawing and heat inactivation of corticosterone binding globulins (65 °C for 20 min), serum baseline and ACTH1–24 stimulated corticosterone concentrations were quantified using an Enzyme-Linked ImmunoSorbent Assay (ELISA) (Diagnostic Systems Laboratories, Webster, TX) and a 96-well plate reader (Molecular Devices, Sunnyvale, CA).
Publication 2009
BLOOD Cardiac Arrest Catheters Centrifugation Clotrimazole Corticosterone Corticotropin Dexamethasone Diagnosis Drug Delivery Systems Enzyme-Linked Immunosorbent Assay Erythrocytes Etomidate Fibrin Flushing Freezing Globulins Heparin Medical Devices methoxycarbonyletomidate Normal Saline Pharmaceutical Preparations Phlebotomy Propofol Propylene Glycol Rattus Serum Tail Veins
This study was designed as a prospective, double‐blinded, randomized, placebo‐controlled, trial. The study design was approved by the ethical committee of the Centre for Clinical Veterinary Medicine Ludwig‐Maximilians‐University, Munich (reference 68‐19‐05‐2016). An informed client consent form was signed by all owners. The dogs were recruited between July 2016 and January 2018 by the same veterinarian (MW) across 4 small animal clinics in Munich, Germany. The randomization list was formed before start of the study through a third person using a research randomizer available on the following website: https://www.graphpad.com/quickcalcs/randomize1.cfm. Dogs of either sex with acute nonhemorrhagic diarrhea between 5 and 40 kg bodyweight, and of at least 9 months of age were enrolled into this study. Only dogs with a fecal consistency score of at least 2 on the CADS‐Index (Table 1) and a duration of gastrointestinal symptoms of <3 days were enrolled. Exclusion criteria were the following: treatment with an antimicrobial within 30 days or treatment with an anti‐inflammatory drug within 7 days before presentation, blood in feces, any signs of systemic inflammation (eg, rectal temperature > 39.0°C [102.2 °F]), severe illness (eg, lethargic mental status, moderate to severe abdominal pain), or significant dehydration prompting hospitalization. These exclusion criteria were chosen to define the disease as “uncomplicated,” thus only dogs that could be treated as outpatients, were included.
The histories of all dogs were recorded in a standardized method with specific questions regarding stress‐related factors, diet, dietary changes, feeding of treats, chronic illnesses, other diseases in the last months before presentation, drug administration and timing of any past diarrheic episode.
Diagnostic work‐up in all dogs before inclusion consisted of a blood count, serum chemistry profile (urea nitrogen, creatinine, SDMA, sodium, chloride, potassium, phosphate, total bilirubin, ALT, ALP, gamma‐GT, AST, GLDH, total protein, albumin, globulin, glucose, alpha‐amylase, lipase, cholesterol, fructosamine, creatine kinase, LDH, calcium, magnesium, triglycerides), and a fecal flotation.
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Publication 2020
Abdominal Pain Albumins alpha-Amylases Animals Anti-Inflammatory Agents Bilirubin BLOOD Body Weight Calcium, Dietary Canis familiaris Chlorides Cholesterol Creatine Kinase Creatinine Dehydration DFFB protein, human Diagnosis Diarrhea Diet Dietary Modification Disease, Chronic Feces Fructosamine gamma-Glutamyl Transpeptidase Globulins Glucose Hematochezia Hospitalization Inflammation Lipase Magnesium Microbicides Nitrogen Outpatients Phosphates Placebos Potassium Proteins Rectum Respiratory Diaphragm Serum Sodium Triglycerides Urea Veterinarian

Most recents protocols related to «Globulins»

The data collected in this retrospective study were obtained through the hospital's electronic medical record system and included baseline information (sex, age, and past medical history), clinic symptoms (main onset phenotype and state of consciousness), laboratory examinations (blood cell count, total protein, Alb, globulin, coagulation function index, CRP, and FARP), electroencephalogram (EEG), magnetic resonance imaging (MRI), and treatment options. Fasting venous blood was collected from the patients early in the morning after admission. All blood samples acquired for routine blood tests and biomarker identification were analyzed in the biochemistry laboratory of the First Affiliated Hospital of Zhengzhou University. All tests were performed according to the manufacturer's instructions and relevant guidelines, and the inspectors were blinded to all clinical information.
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Publication 2023
Biological Markers BLOOD Blood Cell Count Coagulation, Blood Consciousness Electroencephalography Globulins Hematologic Tests Patients Phenotype Physical Examination Proteins Veins
RO3280 (≥99.5%)
and GSK461364 (≥99.8%) were supplied by MedChem Express. HSA
(≥99%; fatty acid- and globulin-free), ibuprofen (>98%),
warfarin
(99.9%), Bis-Tris (≥98.0%), NaCl (≥99.0%), and DMSO
(99.9%) were purchased from Sigma-Aldrich. The samples were dissolved
in 0.02 M Tris-HCl buffer solutions at pH 7.4 containing 0.1 M NaCl.
All of the buffer solutions were prepared in Milli Q water and filtered
with 0.22 μm filters before being used.
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Publication 2023
Bistris Buffers Fatty Acids Globulins GSK 461364 Ibuprofen RO3280 Sodium Chloride Sulfoxide, Dimethyl Tromethamine Warfarin
We extracted demographics and general information including the department of consultation, age at diagnosis, duration of disease, history of smoking, therapy before and after admission, comorbidities and symptoms. Laboratory findings, such as blood cell counts, albumin (ALB), globulin (GLO), C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), lactate dehydrogenase (LDH), creatine kinase (CK), creatine kinase MB (CKMB), myohemoglobin (MB), Neutrophil-to-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), monocyte-lymphocyte ratio (MLR), the CRP to ALB ratio (CAR), the ESR to ALB ratio (EAR), ferritin and serologic autoantibodies were all collected. We also analyzed the imaging findings, such as irregular linear opacities, grid shadow, nodular shadow, septal thickening, ground-glass opacities, patch shadow, traction bronchodilation, honeycombing, and pleural effusion. It is worth emphasizing that an abnormal chest CT scan was defined as any ILD meeting the 2013 American Thoracic Society criteria16 (link). High-resolution CT (HRCT) scans were reevaluated independently by two experienced chest radiologists.
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Publication 2023
Albumins Autoantibodies Blood Cell Count Blood Platelets Chest C Reactive Protein Creatine Kinase Diagnosis Ferritin Globulins Isoenzyme CPK MB Lactate Dehydrogenase Lymphocyte Monocytes Neutrophil Pleural Effusion Radiologist Sedimentation Rates, Erythrocyte Therapeutics Traction X-Ray Computed Tomography
At pre- and post- intervention visits the following assessments were additionally conducted: Migraine Disability Test (MIDAS)74 (link), Headache Impact Test, version 6 (HIT-6)75 (link) and blood draw for biomarker and safety analysis (albumin, Calcium, cortisol, alanine aminotransferase, pancreatic-amylase, alkaline phosphatase, aspartate aminotransferase, beta-hydroxybutyrate, bilirubin, creatine kinase, Chloride, Cholesterol, Cholesterol Quotient, Cortisol basal, high sensitivity-C reactive protein, globulin, fasting glucose, gamma-glutamyl transferase, glomerular filtration rate, uric acid, HbA1c, High density lipoprotein, urea, Potassium, creatinine, lactate plasma, lactate dehydrogenase, low-density lipoprotein (calculated with Friedewald’s equation), Magnesium, Sodium, Phosphate, total protein, triglycerides, leukocyte count, erythrocytes, hemoglobin, hematocrit, mean corpuscular volume, platelets, T3, T4, Insulin and thyroid stimulating hormone (TSH). All blood samples were taken after an overnight fast between 8 and 11 am and all markers were considered in the responder analysis. Further details on data collection are provided in the published study protocol72 (link).
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Publication 2023
3-Hydroxybutyrate Albumins Alkaline Phosphatase alpha-Amylases Aspartate Transaminase Bilirubin Biological Markers BLOOD Blood Platelets Calcium, Dietary Chlorides Cholesterol C Reactive Protein Creatine Kinase Creatinine D-Alanine Transaminase Disabled Persons Erythrocytes Erythrocyte Volume, Mean Cell gamma-Glutamyl Transpeptidase Globulins Glomerular Filtration Rate Glucose GOLPH3 protein, human Headache Hemoglobin High Density Lipoproteins Hydrocortisone Insulin Lactate Lactate Dehydrogenase Leukocyte Count Low-Density Lipoproteins Magnesium Migraine Disorders Phosphates Plasma Potassium Proteins Safety Sodium Thyrotropin Triglycerides Urea Uric Acid Volumes, Packed Erythrocyte

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Publication 2023
Albumins BLOOD Centrifugation Enzyme-Linked Immunosorbent Assay Enzymes Globulins Lipopolysaccharides Mice, House Proteins Serum

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Bovine serum albumin (BSA) is a common laboratory reagent derived from bovine blood plasma. It is a protein that serves as a stabilizer and blocking agent in various biochemical and immunological applications. BSA is widely used to maintain the activity and solubility of enzymes, proteins, and other biomolecules in experimental settings.
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The FITC anti-rabies monoclonal globulin is a laboratory reagent used for the detection and identification of rabies virus. It is a fluorescein isothiocyanate (FITC) conjugated monoclonal antibody that specifically binds to the rabies virus antigen, allowing for its visualization under a fluorescence microscope.

More about "Globulins"

Globulins are a diverse class of proteins found in the blood plasma and other bodily fluids, playing crucial roles in the immune system and various biological functions.
These protein molecules can be further classified into different subtypes, including alpha globulins, beta globulins, and gamma globulins, each with its own unique characteristics and responsibilities.
Alpha globulins, such as serum albumin (e.g., bovine serum albumin and human serum albumin), are involved in maintaining the oncotic pressure of the blood and transporting various substances throughout the body.
Beta globulins, on the other hand, include proteins like transferrin and C-reactive protein, which are involved in iron transport and the acute-phase response, respectively.
Gamma globulins, often referred to as immunoglobulins, are the antibodies produced by the body's immune system to recognize and neutralize foreign substances, such as pathogens.
These globulins play a crucial role in the adaptive immune response and are essential for maintaining overall health and well-being.
Researchers studying globulins can leverage powerful AI-driven platforms like PubCompare.ai to optimize their research workflows.
These platforms allow scientists to easily locate relevant protocols from the literature, preprints, and patents, and use advanced AI-powered comparisons to identify the best products and methods to ensure reproducibility and drive their research forward.
Analytical instruments like the VetScan VS2, ProCyte Dx, AU5800, BD Vacutainer, VetScan VS2 Chemistry Analyzer, AU680, and Cobas 8000 are commonly used to measure and analyze various globulin subtypes in clinical and research settings.
Additionally, techniques such as FITC anti-rabies monoclonal globulin are employed to detect and quantify specific immunoglobulins.
By understanding the diverse roles and characteristics of globulins, researchers can make informed decisions and utilize the latest advancements in technology to enhance their studies, ultimately contributing to the advancement of scientific knowledge and improved healthcare outcomes.