Ferritin Quantitative Test

HbA1c Rapid Quantitative Test (Chemiluminescence Immunoassay)

HbA1c Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the Glycated hemoglobin A1c (HbA1c) concentration in human whole blood that contains EDTA or without anticoagulants samples, mainly used for the supervising of long-term glycemic control in diabetic individuals and auxiliary diagnosis of diabetes and identify patients at risk of diabetes.

Product Detail

Application

HbA1c is a product of the non-enzymatic chemical reaction between glucose and the N-terminus of the hemoglobin protein's β-chain (valine) amino groups. From a molecular biology perspective, HbA1c belongs to a diverse group of molecules termed advanced glycation end-products (AGEs).

 

In both diabetic and non-diabetic individuals, the relative levels of HbA1c reflect the duration and severity of hyperglycemic episodes, as well as the overall exposure to extracellular glucose present in the circulation. HbA1c levels, at varying cut-offs, have been developed as biomarkers for both the diagnosis of diabetes and the assessment of chronic glycemic control.

 

HbA1c reflects the average plasma glucose concentration over the previous 8 to 12 weeks. It can be measured at any time of the day and does not require special preparation, such as fasting. These properties have made HbA1c the preferred test for assessing glycemic control in people with diabetes.

 

More recently, there has been substantial interest in using HbA1c as a diagnostic test for diabetes and as a screening test for individuals at high risk of developing the condition. The use of HbA1c can avoid the problem of day-to-day variability in glucose values and eliminates the need for fasting and preceding dietary preparations. These advantages have important implications for the early identification and treatment of diabetes, which have been strongly advocated in recent years.

 

A persistently elevated level of HbA1c increases the risk of various vascular complications, such as coronary disease, heart attack, stroke, heart failure, kidney failure, blindness, erectile dysfunction, neuropathy, gangrene, gastroparesis, and short-term complications of surgery, including poor wound healing.

 

Product Specification

Sample Volume

WB: 10μL

Test Time

15 mins

Measuring Range

4.2-20%

Pack

20T、40T、100T

Storage

2~30℃

 

Features

Smart - Photosensitive and Luminescent Microspheres

Rapid - Whole Blood Sample Type Supported & No Centrifuge Needed

Convenient - Room Temperature Storage & Minimal sample consumption

 

Clinical significance

Diagnosis and Monitoring of Diabetes

Assessment of Long-Term Blood Glucose Control

Cardiovascular Risk Assessment

Medication Adjustment and Treatment Planning

Screening for Prediabetes

Leave A Message

Please provide us with the information below, and we'll contact you as soon as possible.

Related Products
C-peptide Rapid Quantitative Test (Chemiluminescence Immunoassay)
C-peptide Rapid Quantitative Test (Chemiluminescence Immunoassay)
C-peptide Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the C-peptide concentration in human serum and plasma that contains heparin /EDTA and other anticoagulants samples, mainly used for auxiliary diagnosis of diabetes diseases.
INS Rapid Quantitative Test (Chemiluminescence Immunoassay)
INS Rapid Quantitative Test (Chemiluminescence Immunoassay)
INS Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the Insulin (INS) concentration in human serum, plasma that contains heparin /EDTA and other anticoagulants samples, mainly used for auxiliary diagnosis of diabetes diseases.
biotime AFP Rapid Quantitative Test
AFP Rapid Quantitative Test
Alpha-fetoprotein (AFP) is a protein produced primarily by the liver in a developing baby (fetus) and the portion of a developing embryo that is similar to the yolk cavity in bird eggs (yolk sac tissues). AFP levels are typically elevated when a baby is born and then decline rapidly.
HSV-2 IgG/IgM Rapid Test (Fluorescence Immunoassay)
HSV-2 IgG/IgM Rapid Test (Fluorescence Immunoassay)
The HSV-2 IgG/IgM Rapid Test is an in vitro immunoassay for the qualitative determination of IgG and IgM class antibodies to HSV2 in human serum. The test is intended for use as an aid in the assessment of immune status and as an aid in the diagnosis of HSV infection. The HSV-2 IgM test shall not be used for prenatal screening of asymptomatic people, and the test results of this reagent shall not be used alone as the basis for termination of pregnancy. -Fluorescent immunoassay -Herpes simplex viruses2 (HSV-2) infection -For in vitro diagnostic use only. For professional use only.
H. Pylori Antigen Qualitative Test(Fluorescence Immunoassay)
H. Pylori Antigen Qualitative Test(Fluorescence Immunoassay)
The Biotime Helicobacter pylori (H.pylori) Antigen Rapid Test is intended to qualitatively detect the Helicobacter pylori (H.pylori) antigen in human faeces samples on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an early aid diagnosis and screening of  Helicobacter pylori infection. For in vitro diagnostic use only. For professional use only.
biotime HCV Rapid Quantitative Test
HCV Rapid Quantitative Test
Hepatitis C is a liver disease caused by the hepatitis C virus (HCV): the virus can cause both acute and chronic hepatitis, ranging in severity from a mild illness lasting a few weeks to a serious, lifelong illness. Hepatitis C is a major cause of liver cancer.
LH Rapid Quantitative Test (Chemiluminescence Immunoassay)
LH Rapid Quantitative Test (Chemiluminescence Immunoassay)
LH Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the Luteinizing hormone (LH) concentration in human serum and plasma that contains heparin /EDTA and other anticoagulants samples, mainly used for auxiliary diagnosis of reproductive hormones diseases.
Biotime PROG Rapid Quantitative Test
PROG Rapid Quantitative Test
Progesterone(PROG) is produced by the corpus luteum or in females, the male progesterone level is very low and mainly produced by adrenal cortex. Biotime PROG test is used for determining ovulation, monitoring progesterone therapy and evaluating early pregnancy status.
Leave A Message

Leave A Message

    Please provide us with the information below, and we'll contact you as soon as possible.

Home

products

about

contact