Fatigue Wellness

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This test is intended for the quantitative determination of Vitamin B12 level in human serum. Accurate measurement of Vitamin B12 levels in patients is very important for the diagnosis of Vitamin B12 deficiency and for the monitoring of deficient patients in order to achieve optimal levels. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Recommended test for suspected Vitamin B12 deficiency related anemia and pernicious anemia, loss of balance, numbness or tingling in the arms and legs, and weakness. Initial laboratory tests for suspected Vitamin B12 deficiency should include measurement of Vitamin B12 serum levels by ELISA immunoassay and a complete blood cell count. In patients that present with symptoms of deficiency but have normal B12 serum levels, or are considered “high risk” but are asymptomatic, measurement of homocysteine and/or methylmalonic acid in the serum may also be used to confirm deficiency.

Features:

• Specificity: No cross-reactivity with bilirubin, cobinamide, hemoglobin, lipemia, or RF
• Intra-assay Precision: CV ≤ 7.3%
• Inter-assay Precision: CV ≤ 11.6%
• Stabilizing Agent
• VB12 Enzyme Reagent
• VB12 Biotin Reagent
• Neutralizing Buffer
• Releasing Agent
• Wash Buffer (50X Concentrate)
• TMB Substrate
• Stop Solution
• Product Insert

VB12 Calibrators: 

• C1 (0 pg/mL)
• C2 (100 pg/mL)
• C3 (200 pg/mL)
• C4 (400 pg/mL)
• C5 (1000 pg/mL)
• C6 (2000 pg/mL)

The four main kit components are:

• A 96-well breakable solid microwells pre-coated with streptavidin
• Vitamin B12 (VB12) Calibrators
• VB12 Biotin Reagent comprised of anti-Vitamin B12 biotinylated purified rabbit IgG conjugate
• VB12 Enzyme Reagent comprised of Vitamin B12 analog-HRP conjugate in a protein stabilizing matrix

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This test is intended for the quantitative determination of Vitamin D level in human serum. Accurate measurement of Vitamin D levels in patients is very important for the diagnosis of Vitamin D deficiency and for the monitoring of deficient patients in order to achieve optimal levels. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Recommended test for suspected Vitamin D deficiency related rickets, osteomalacia, and osteoporosis, as well as fetal development, immune system function, neurological disorder such as multiple sclerosis, cancer and many other pathologies. Initial laboratory tests for suspected Vitamin D deficiency. The 25(OH)D is the major circulating form and stays constant in the body for longer, so it is the most accurate and therefore most common biomarker of Vitamin D status. The sum of 25(OH)D in serum or plasma is referred to as total 25(OH) Vitamin D.

The five main kit components are:

• Solid microwells pre-coated with anti-Vit D antibody
• Vit D Calibrators
• Vit D Assay Controls comprised of human serum with the Vit D concentration on  the label. Contains preservative. Store at 2-8℃.
• Vit D Releasing Agent comprised of Vitamin D binding protein releasing agents, and
• Vit D Enzyme Reagent comprised of 25-OH Vitamin D3 analog-HRP conjugate in a protein stabilizing matrix.

• Cross-Reactivity: Reaction with 25(OH)D3, 25(OH)D2, 1,3,25(OH) D3. No cross-reactivity with Vitamin D2 and D3
• Intra Assay Precision: CV ≤ 7.40%
• Inter Assay Precision: CV ≤ 9.17%
• Vit D Assay Control A
• Vit D Assay Control B
• Vit D Releasing Agent
• Vit D Enzyme Reagent
• Wash Buffer (50X Concentrate)
• TMB Substrate
• Stop Solution
• Product Insert

• C1 (0 ng/mL)
• C2 (5 ng/mL)
• C3 (10 ng/mL)
• C4 (25 ng/mL)
• C5 (46 ng/mL)
•  C6 (85 ng/mL)
• C7 (150 ng/mL)