Vibrant Wellness & America are no longer available on platforms like Rupa, but we’ve created a list of comparable tests. You can also talk to a Rupa rep to help you transition to alternatives! Learn more.
This panel is designed to detect Lyme Disease. It combines 4 tests: Lyme ImmunoBlot IgM & IgG, Lyme Multiplex PCR – Whole Blood, and Lyme Multiplex PCR – Serum. This test is unavailable for patients over 65 when ordered through physician services.
To help you choose the best test for your patients, we’ve built lab test comparisons! Select any lab tests to compare up to 18 key characteristics between them. You also have the ability to copy & share a link to your comparisons to anyone inside or outside of Rupa!
Lyme Disease Antibody w/ Reflex to Blot (IgG, IgM)
by
Access Med Labs
Serum
This test detects antibodies to the bacterium Borrelia burgdorferi. Lyme disease is caused by Borrelia burgdorferi and is transmitted to humans through the bite of infected black-legged ticks. Immunoblot testing will confirm a detected screening result.
Epstein-Barr Virus (EBV) Panel
by
Immunosciences Lab
Serum
EBV contributes to more than 30 autoimmune disorders. Detection of IgG or IgM antibodies to various EBV antigens indicates either past infection, primary reactivation, or re-infection with Epstein-Barr Virus or Herpes Type 4.
Immunoserology of Lyme Panel B
by
Immunosciences Lab
Serum
This panel uses Immunosciences Lab's patented ELISA methodology, as well as the Western Blot technique, to measure 26 different antibodies against Lyme-specific antigens, Borrelia subspecies, and co-infections. It can detect active and chronic Lyme disease, including Lyme arthritis and neuroborreliosis that may be confused with multiple sclerosis.
B. burgdorferi IgG, IgM by Western Blot
by
Immunosciences Lab
Serum
This test confirms the presence of ongoing Lyme disease based on CDC criteria.
Lyme Disease, Line Blot
by
Labcorp
Serum
This test is used to detect antibodies specific for B. burgdorferi. This test is intended as the second step in testing serum samples found to have been equivocal or positive using an ELISA or IFA test.
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