Eagle Biosciences, Inc. has teamed up once again with Immundiagnostik to bring it’s customers a series of zonulin ELISA’s. These ELISA’s are used for the quantitative determination of zonulin in serum or stool samples. 

Zonulin is a novel human protein analogue to the zonula occludens toxin derived from Vibrio cholerae which participates in tight junctions between cells of the wall of the digestive tract. Zonulin binds to a specific receptor on the surface of intestinal epithelia and triggers a cascade of biochemical events which induces tight junction disassembly and a subsequent permeability increase of the intestinal epithelia, allowing some substances to pass through and activate immune reactions.

Dr. Fasano and his co-workers found out that the zonulin-zonulin-receptor-system is
more activated in celiac disease and type 1 diabetes mellitus patients. Patients with
active celiac disease showed higher levels of zonulin and anti-zonulin antibodies
compared to non-celiac patients and patients in remission, who were on a glutenfree
diet. 

Concerning the autoimmune type 1 diabetes, in experiments with rats it could be
demonstrated that elevated zonulin levels as well as increased intestinal permeability
precede a type 1 diabetes disease. Conversely, type 1 diabetes could be prevented
by inhibition of zonulin in animal experiments.


In addition, it was reported that many people who suffer from celiac disease also suffer
from other autoimmune disorders. It is suggested that increased levels of zonulin
are a contributing factor to the development of celiac disease and other autoimmune
disorders such as insulin dependent diabetes, multiple sclerosis and rheumatoid
arthritis.

Serum and Stool Zonulin ELISA’s are available now! 

References: 

1. Fasano, A, T Not, W Wang, S Uzzau, I Berti, A Tommasini, and S E Goldblum. 2000.
“Zonulin, a Newly Discovered Modulator of Intestinal Permeability, and Its Expression
in Coeliac Disease.” Lancet 355 (9214) (April 29): 1518–9. doi:10.1016/S0140-
6736(00)02169-3. 

2. Wang, W, S Uzzau, S E Goldblum, and A Fasano. 2000. “Human Zonulin, a Potential
Modulator of Intestinal Tight Junctions.” Journal of Cell Science 113 Pt 24 (December):
4435–40. 

3. Fasano, A. 2001. “Intestinal Zonulin: Open Sesame!” Gut 49 (2) (August): 159–62. 

4. Freemark, Michael, and Lynne L Levitsky. 2003. “Screening for Celiac Disease in
Children with Type 1 Diabetes: Two Views of the Controversy.” Diabetes Care 26 (6)
(June): 1932–9.
Manual IDK® Zonulin ELISA
24 

5. Lazzarotto, Francesca, Daniela Basso, Mario Plebani, Alessandro Moscon, Renato
Zanchetta, and Corrado Betterle. 2003. “Celiac Disease and Type 1 Diabetes.” Diabetes
Care 26 (1) (January): 248–9. 

6. Watts, Tammara, Irene Berti, Anna Sapone, Tania Gerarduzzi, Tarcisio Not, Ronald
Zielke, and Alessio Fasano. 2005. “Role of the Intestinal Tight Junction Modulator
Zonulin in the Pathogenesis of Type I Diabetes in BB Diabetic-Prone Rats.” Proceedings
of the National Academy of Sciences of the United States of America 102 (8)
(February 22): 2916–21. doi:10.1073/pnas.0500178102. 

7. De Magistris, Maria Teresa. 2006. “Zonula Occludens Toxin as a New Promising
Adjuvant for Mucosal Vaccines.” Vaccine 24 Suppl 2 (April 12): S2–60–1. 

8. Sapone, Anna, Laura de Magistris, Michelle Pietzak, Maria G Clemente, Amit Tripathi,
Francesco Cucca, Rosanna Lampis, et al. 2006. “Zonulin Upregulation Is Associated
with Increased Gut Permeability in Subjects with Type 1 Diabetes and Their
Relatives.” Diabetes 55 (5) (May 1): 1443–9. doi:55/5/1443 [pii]. 

9. Thomas, Karen E, Anna Sapone, Alessio Fasano, and Stefanie N Vogel. 2006. “Gliadin
Stimulation of Murine Macrophage Inflammatory Gene Expression and Intestinal
Permeability Are MyD88-Dependent: Role of the Innate Immune Response
in Celiac Disease.” Journal of Immunology (Baltimore, Md. : 1950) 176 (4) (February
15): 2512–21.

In a recent study released by AroCell, the novel proliferation biomarker, Thymadine Kinase 1, is proving to provide more information to researchers studying more than hematological malignancies. With the help of AroCells TK 210 ELISA, there are reports that this test can complement the PSA-related biomarkers that are used to help diagnose prostate cancer.

“The main objective of this study is to determine if TK 210 ELISA can complement the PSA-ralated biomarkers leading to a higher specificity and sensitivity in the diagnosis of prostate cancer.” the objective states in newly released research poster. AroCell TK 210 ELISA May Complement Pro PSA and the Prostate Health Index in Differentiating Non-Cancerous from Cancerous Conditions in Prostate Disease (Jagarlamudi, KK et al.).

“The results indicate that the AroCell TK 210 kit can aid in differentiating the non-cancerous group from the confirmed PCa group in urology patients with PSA values between 2 to 10 µg/L.” the poster continues, “Further clinical studies are needed to establish the role of TK 210 ELISA as a complement to pro PSA and PHI, which could be a valuable tool in prostate cancer diagnosis.”

We at Eagle Biosciences, Inc are Proud to Announce an Exclusive Partnership with Kyowa Medex Co., Ltd from Tokyo, Japan!


 

MedFrontier FGF-23 provides a simpler and quicker assay procedure that yields a broader dynamic range than it’s competitors 

 

About the NEW MedFrontier FGF23 ELISA Kit…

MedFrontier FGF-23 is a sandwich ELISA kit that measures only intact/active forms of FGF23. Manufactured by Kyowa Medex Co. of Tokyo, Japan, the MedFrontier FGF23 is the only kit of its kind. Studying intact FGF23 has shown to provide greater accuracy when researching the importance of this protein.

Dynamic Range 15-3000 pg/mL
Incubation Time ~2 hours
Sample Size 20 µL
Sample Type Serum

What is FGF23?

Fibroblastic Growth Factor 23 (FGF23) is a hormone that is secreted by osteoblasts with the bones. This protein works primarily with the kidneys to help regulate levels of phosphate within the bloodstream via signals for removal or reabsorbtion. The parathyroid and digestive system also aid in phosphates homeostasis within the body. The kidneys remove excess phosphate through waste, and reabsorbs it via the small intestines when needed.


Why Measure FGF23?

Phosphate plays a critical role in the formation and growth of bones in children and maintaining strength in adults. If there is an imbalance of FGF23 within the bloodstream, it can cause hyper- and hypophosphatemia. These conditions have been linked to Rickets, osteomalacia, and impaired renal function to name a few.

 

What Is It?

This Eagle Biosciences High Sensitivity Glucagon ELISA Assay Kit is used for quantitative determination of glucagon in plasma, serum and culture medium supernatant. The kit is characterized by its sensitive quantification and high specificity. In addition, it has no influence by other components in samples.


How Does It Work?

This ELISA kit for determination of glucagon is based on a sandwich enzyme immunoassay with two monoclonal antibodies. Standards or samples, and HRP labeled antibodies are added to the wells of plate coated with antibodies against glucagon. During the incubation antibody – antigen – labeled antibody complex is formed on the surface of the wells. After the incubation and rinsing out excess labeled antibody, HRP enzyme activity is finally determined by 3,3’,5,5’-Tetramethylbenzidine (TMB) and the concentration of glucagon is calculated.

What Is It’s Specifity?

This Eagle Biosciences High Sensitivity Glucagon ELISA Assay Kit has high specificity to glucagon, and shows no significant cross reactivity to Glicentin, Oxyntomodulin, GLP-1 and GLP-2.

 

 

For more information or purchasing of this product, visit here

NT-proCNP ELISA Assay Kit is for the quantitative determination of human NT-proCNP in plasma and serum samples. 

Important Factors:

  • Extensively validated for serum and plasma samples (more info here)
  • Reliable– 7 human serum based standards and 2 controls for biologically reliable data. 
  • Robust– Excellent stability in all matrices after sample collection 
  • Easy– Conventional 96-well format 

This ELISA has many areas of interest in the study of vascular disease, growth, angiogenesis, spesis, and skeletal development

This ELISA is manufactured by Biomedica and intended for research use only  

For more information visit Eagle Biosciences NT-proCNP ELISA Assay Kit’s Product Page

Vitamin-D Could Help Patients with Insomnia

In a new study released by Nutritional Neuroscience, Vitamin D supplements may increase quality of sleep in some patients. A double blind, clinical trial was conducted on 89 people between 20-50 years old. The patients were divided into two groups; 44 who will take at least 50,000 units of vitamin D for 8 weeks, and 45 people who will take a placebo. In order to understand each patients quality of sleep they all performed a Petersburg’s Sleep Quality QuestionnaireInternational Physical Activity Questionnaire, general information questionnaire, sun exposure, vitamin D serum level and 3-day food record questionnaire both before and after the study. 

The results of this study showed that a decrease in vitamin D levels also decreases the quality of sleep a patient has. Those patients that took the vitamin D supplements showed a decrease in sleep latency, as well as a better sleep score than those who took a placebo. The conclusion of this study shows promising insight into future studies as ways to help those who suffer from a diagnosed sleep disorder with the use of vitamin D therapies. 


Sources: 
The effect of vitamin D supplement on the score and quality of sleep in 20–50 year-old people with sleep disorders compared with control group. (2017). Nutritional Neuroscience. Retrieved from https://www.tandfonline.com/doi/abs/10.1080/102841…

Eagle Biosciences Welcomes Another Product to the Endocrinology ELISA Product Line!

 

A Little Bit About Pancreatic Elastase…

Pancreatic elastase is an anionic endoprotease of the serine protease family with a molecular weight of 26 kDa. Together with other digestive enzymes it is synthesized as an inactive pro-enzyme in the acinar cells of the pancreas and is secreted into the duodenum. After its activation, pancreas elastase cleaves peptides after neutral amino acids. Pancreas elastase is mainly bound to bile salts during intestinal passage and is not degraded. In human feces it is 5–6 fold more concentrated than in pancreatic juice. The stool concentration reflects the secretory capacity of the pancreas.

What You Can Expect…

The Eagle Biosciences Pancreatic Elastase ELISA Assay Kit is intended for the quantitative determination of human pancreatic elastase in stool. This kit is for research use only and should not be used in therapeutic procedures. The Eagle Biosciences Pancreatic Elastase ELISA Assay Kit is intended for the quantitative determination of pancreatic elastase in stool. In a first incubation step, the pancreatic elastase in the samples is bound to monoclonal antibodies, immobilized to the surface of the microtiter wells. To remove all unbound substances, a washing step is carried out. In a second incubation step, a peroxidase-labeled conjugate (mouse anti pancreatic elastase) is added which recognizes specifically the bound pancreatic elastase. After another washing step to remove all unbound substances, the solid phase is incubated with the substrate, tetramethyl-benzidine (TMB), which reacts with the peroxidase. An acidic stop solution is added to stop the reaction. The color changes from blue to yellow. The intensity of the yellow color is directly proportional to the concentration of pancreatic elastase. A dose response curve of absorbance unit (optical density, OD at 450 nm) vs. concentration is generated using the values obtained from the standards. Pancreatic elastase present in the patient samples is determined directly from this curve.

Check out this and all of our other Endocrine ELISA’s Here

We at Eagle Biosciences are Proud to Introduce a New ELISA to Our Endocrinology Product Line:

 

Human Anti-Müllerian Hormone ELISA Assay Kit

 

What is Anti-Müllerian Hormone (AMH)?

Anti-Müllerian Hormone (AMH) or Müllerian-inhibiting hormone (MIH) is a glycoprotein hormone structurally related to inhibin and activin from the transforming growth factor beta superfamily, whose key roles are in growth differentiation and folliculogenesis. AMH expression is critical to sex differentiation at a specific time during fetal development, and appears to be tightly regulated by nuclear receptor SF1, transcription GATA factors, sex-reversal gene DAX1, and follicle-stimulating hormone
(FSH). AMH is activated by SOX9 in the Sertoli cells of the male fetus thereby
arresting the development of fallopian tubes, uterus, and upper vagina. AMH is
also a product of granulosa cells of the preantral and small antral follicles
in women. As such, AMH is only present in the ovary until menopause. AMH can
serve as a molecular biomarker for relative size of the ovarian reserve and can
also be used as a marker for ovarian dysfunction, such as in women with
polycystic ovary syndrome (PCOS).

 

What Makes Eagle Biosciences AMH Assay Different?

Compared to other products on the market, our Anti-Müllerian Hormone ELISA Assay Kit provides a much simpler procedure with less washes and incubation time. Eagle Biosciences Human Anti-Müllerian Hormone ELISA Assay kit is intended for use in the quantitative determination of human Anti-Mullerian Hormone (AMH) levels in serum, EDTA plasma and lithium heparin plasma samples.

Size 1×96 wells
Sensitivity 0.02 ng/mL
Dynamic Range 0.11-20 ng/mL
Incubation Time 4.5 hours
Sample Type Serum/Plasma
Sample Size 50 µL

 

Supporting Resources: 

Broer, S., Broekmans, F., Laven, J. and Fauser, B. (2014). Anti-Müllerian hormone: ovarian reserve testing and its potential clinical implications. Human Reproduction Update, 20(5), pp.688-701.

Dewailly, D., Andersen, C., Balen, A., Broekmans, F., Dilaver, N., Fanchin, R., Griesinger, G., Kelsey, T., La Marca, A., Lambalk, C., Mason, H., Nelson, S., Visser, J., Wallace, W. and Anderson, R. (2014). The physiology and clinical utility of anti-Müllerian hormone in women. Human Reproduction Update, 20(3), pp.370-385.

Dumont, A., Robin, G., Catteau-Jonard, S. and Dewailly, D. (2015). Role of Anti-Müllerian Hormone in pathophysiology, diagnosis and treatment of Polycystic Ovary Syndrome: a review. Reproductive Biology and Endocrinology, 13(1).

EagleBio’s Adrenaline, Nonadrenaline, and Dopamine ELISA Assay, was recently used in an environmental study. This assay is a part of our Neurobiology Assay Kit line which is comprised of a unique set of products that can ve used in a variety of applications, research, and fields of study. Check out the product page for full details on this kit, or click the below to check out the new publications referencing our Adrenaline, Nonadrenaline, Dopamine ELISA Assay.

Egorov, Andrey I., et al. “Vegetated land cover near residence is associated with reduced allostatic load and improved biomarkers of neuroendocrine, metabolic and immune functions.” Environmental Research, vol. 158, Oct. 2017, pp. 508-521., https://www.sciencedirect.com/science/article/pii/S0013935117304826

“Greater exposure to urban green spaces has been linked to reduced risks of depression, cardiovascular disease, diabetes and premature death. Alleviation of chronic stress is a hypothesized pathway to improved health. Previous studies linked chronic stress with a biomarker-based composite measure of physiological dysregulation known as allostatic load.” Read More. 

Join Us for a Special Webinar Featuring the New TK 210 ELISA Assay Kit

Wednesday, November 15, 2017 at 10:00 AM EST

REGISTER HERE

 


AroCell TK 210 ELISA:

A Novel Proliferation Biomarker to 

Study Hematological Malignancies

Thymidine Kinase 1 (TK1) has been long known as a valuable biomarker of cellular proliferation. However, previous methods have been based on enzyme activity measurements that are complex and require specialized equipment. Introducing the AroCell TK 210 ELISA as a new valuable assay for TK1 that brings the simplicity and robustness in a widely available assay kit (sold only in the US by Eagle Biosciences). Based on unique monoclonal antibodies (TK 210 epitope), the AroCell TK 210 ELISA Assay Kit creates an easy to use assay and provides new opportunities for studying cellular proliferation, tumor cell turnover and therapy response in subjects with hematological malignancies. 

During this webinar, you will learn the importance of proliferation biomarkers, and their key role in monitoring malignancies, as well as the aiding in making prognoses which could provide early insights into the effects of therapy. Since Thymidine kinase 1 (TK1) is a well-known proliferation biomarker, studying this biomarker has been based on enzyme activity methods and may underestimate serum TK1 levels, particularly in subjects with solid tumors. Improved immunoassays of TK1 based on the TK 210 antigen (AroCell TK 210 ELISA) has shown promising insight of studying these hematological malignancies. 

 

Meet the Speakers: 

Staffan Eriksson | Professor in Medical and Physilogical Chemistry at the

Swedish University of Agricultural Sciences

Steffan Eriksson has been active in the research of medical biochemistry and Thymidine Kinase for many decades, and has published over 120 scientific studies related to these topics. He is also founder of AroCell AB and one of the inventors of the TK 210 ELISA Assay test for measuring cell grown and turnover. 

 

Martin Shaw | AroCell Development Manager

Martin Shaw has had a long experience in the development and application of many novel biomarkers. He has participated in industry-wide consortia on the qualification of biomarkers for application in pre-clinical and clinical trials. He has spoken at many congresses including being a guest speaker at the FDA. 

 

We Hope You Can Join Us!

 

 

If you would like to receive a white paper on the use of TK1 and TK 210
ELISA in studying hematological malignancies, please 
click here