
Human Serum Coombs Antisera (Antihuman Globulin Reagent)
Pack Sizes Available
Product Description
Technical Specifications
- Reagent Type: Antihuman globulin (AHG) reagent / Coombs reagent
- Specificity: Polyspecific: Anti-IgG and Anti-C3d (detects both IgG antibodies and complement component C3d)
- Production Method: Polyclonal antibodies produced by immunizing animals (rabbits) with human immunoglobulins
- Presentation: Liquid reagent in dropper bottle, dyed green (patent blue + tartrazine) for identification
- Drop Volume: Approximately 40 µL per drop from dropper bottle
- Preservative: 0.1% (w/v) sodium azide
- Storage Temperature: 2-8°C (refrigerated), do not freeze
- Shelf Life: 18-24 months from date of manufacture when stored properly
- Clinical Applications: Direct Antiglobulin Test (DAT), Indirect Antiglobulin Test (IAT), pre-transfusion testing, antibody screening, crossmatching, prenatal screening
- Specimen Type: Washed red blood cells (for DAT) or serum/plasma incubated with reagent RBCs (for IAT); EDTA anticoagulant preferred
- Result Interpretation: Agglutination = positive (antibodies or complement present); No agglutination = negative
- Quality Control: Must be tested with IgG-coated and C3d-coated control cells to verify potency before use
- Regulatory Status: In vitro diagnostic use only, meets FDA/regulatory standards for blood grouping reagents
Frequently asked questions
Coombs antisera (antihuman globulin or AHG reagent) is used in direct and indirect antiglobulin tests (Coombs tests) to detect antibodies and complement components on red blood cell surfaces or in serum. The direct test (DAT) is used to diagnose autoimmune hemolytic anemia, hemolytic transfusion reactions, and hemolytic disease of the newborn. The indirect test (IAT) is used for pre-transfusion antibody screening, blood compatibility testing, and prenatal screening of pregnant women for antibodies that could cause fetal hemolysis.
Polyspecific Coombs antisera contains antibodies against both IgG immunoglobulins and C3d complement component, providing broad detection of either antibody-coated or complement-coated red blood cells. Monospecific antisera contains antibodies against only one target: either anti-IgG (detects only IgG antibodies) or anti-C3d (detects only complement). When polyspecific reagent gives a positive result, monospecific reagents are used for follow-up testing to determine whether cells are coated with IgG, complement, or both, which helps establish clinical significance.
Coombs antisera is produced by injecting animals (typically rabbits or other laboratory animals) with human immunoglobulins (IgG and complement proteins). The animals' immune systems recognize these human proteins as foreign and produce polyclonal antibodies specific for human immunoglobulins and complement factors. These animal antibodies are then harvested, purified, and formulated into the reagent. More specific reagents using monoclonal antibodies can also be produced for targeted applications.
Red blood cells must be thoroughly washed with saline before the direct antiglobulin test to remove the patient's own plasma and any unbound antibodies. If plasma proteins and free antibodies are not removed, they can neutralize the Coombs antisera before it can bind to antibodies on the red cell surface, causing a false-negative result. The washing step ensures that only antibodies actually bound to red blood cells will be detected. Typically, cells are washed 3-4 times with saline.
False-positive results can occur due to: strong cold autoagglutinins that cause rouleaux formation, contamination with Wharton's jelly in cord blood samples, testing clotted blood specimens instead of anticoagulated samples, recent high-dose intravenous immune globulin administration, medications that cause drug-induced antibodies, and certain infections (HIV, malaria, hepatitis C). Proper specimen collection in EDTA tubes, appropriate washing techniques, and awareness of the patient's clinical history help reduce false positives.
Coombs antisera should be stored refrigerated at 2-8°C and must not be frozen, as freezing denatures the antibody proteins. The reagent typically has a shelf life of 18-24 months from the date of manufacture when stored properly. Do not use the reagent beyond its expiration date or if it appears turbid (cloudy), as turbidity indicates contamination or protein aggregation. The reagent contains sodium azide preservative (0.1% w/v) which prevents bacterial growth during storage.

Microlisa HIV Ag & Ab 4th Generation ELISA Test Kit
Blood screening exists in a category of laboratory work where the margin for error is not just professionally unacceptable but medically catastrophic. A false negative in HIV screening does not just fail a test. It compromises patient safety, undermines transfusion protocols, and exposes healthcare systems to risks that nobody wants to calculate. Microlisa HIV Ag & Ab 4th Generation ELISA was engineered to close the detection window that makes early HIV infection so difficult to identify reliably. This is an in-vitro qualitative enzyme immunoassay designed for simultaneous detection of antibodies to HIV-1 (including Group O and subtype C prevalent in India), HIV-2, and HIV-1 p24 antigen in human serum or plasma. The test is intended for screening of blood donors, diagnostic testing of individuals at risk for HIV infection, and clinical evaluation of patients with AIDS-related symptoms. It represents the fourth generation of HIV ELISA technology, which detects both antibodies and antigens simultaneously rather than antibodies alone. The clinical advantage of 4th generation testing is the shortened window period. Traditional antibody-only tests miss early seroconversion cases where HIV-1 p24 antigen is present but antibodies have not yet developed to detectable levels. By detecting p24 antigen during the acute infection phase (typically 2 to 4 weeks post-exposure), this assay identifies infections approximately 1 to 2 weeks earlier than 3rd generation antibody-only tests. That earlier detection matters critically in blood donor screening and post-exposure monitoring. The assay is based on sandwich ELISA methodology. Microtiter wells are pre-coated with HIV envelope proteins (gp41, C-terminus of gp120 for HIV-1, and gp36 for HIV-2) and anti-p24 monoclonal antibodies. When specimens are added, any HIV antibodies or p24 antigen present bind to the coated antigens or antibodies. After washing, horseradish peroxidase (HRPO) conjugated antigens and anti-p24 antibodies are added, forming a sandwich complex. The colorimetric reaction develops proportionally to the amount of HIV antibodies or antigen present, read at 450nm absorbance. The kit uses color-coded reagents to monitor procedural steps, reducing protocol errors during multi-step workflows. Breakaway microwell strips allow testing flexibility from single specimens to full 96-well plate runs. Storage stability is maintained at 2-8°C with a shelf life of 24 months unopened. Total assay time including incubation steps is approximately 120 minutes. Sensitivity and specificity meet international standards for 4th generation HIV screening. Clinical evaluations demonstrate 100% sensitivity in detecting seroconversion panels and p24 antigen standards quantified down to 200 pg/ml. Specificity exceeds 99.5% when tested against large sample populations. The test detects all major HIV-1 subtypes including Group O and subtype C, which are epidemiologically significant in the Indian subcontinent. For distributors supplying blood banks, transfusion centers, diagnostic laboratories, and public health screening programs, Microlisa HIV Ag & Ab represents a clinically validated 4th generation screening platform with predictable reorder cycles. Sara Wellness has been exporting in-vitro diagnostic kits and laboratory reagents from India for 15 years.

Advantage PAN Malaria Card Rapid Diagnostic Test Kit
Malaria diagnosis in endemic regions operates under time pressure that microscopy cannot always accommodate. A patient presenting with fever in a rural health center at midnight does not have the luxury of waiting until morning for a trained microscopist to arrive, prepare slides, and spend twenty minutes examining blood films under oil immersion. That delay can mean the difference between timely artemisinin treatment and cerebral malaria developing overnight. Advantage PAN Malaria Card was designed to deliver species-level diagnosis in settings where microscopy is impractical or unavailable. This is a rapid visual immunoassay for qualitative detection of all four human Plasmodium species (P. falciparum, P. vivax, P. malariae, P. ovale) based on pan-specific plasmodium lactate dehydrogenase (pLDH) antigen in whole blood. The test provides results within 20 minutes using a simple fingerstick blood sample, no laboratory equipment required, making it ideal for point-of-care testing in primary health centers, rural clinics, field hospitals, and outbreak response settings. The assay is based on sandwich immunochromatography using monoclonal antibodies specific to pLDH, an enzyme produced by all Plasmodium species during their erythrocytic life cycle. When infected blood is added to the test device and assay buffer is applied, red blood cells lyse and pLDH antigen (if present) binds to gold-conjugated anti-pLDH antibodies. This complex migrates along the nitrocellulose membrane and is captured by immobilized anti-pLDH antibodies at the test line, producing a visible pink-purple band that confirms malaria infection. The see-through device design allows direct visualization of sample migration and result development, which helps identify invalid tests caused by insufficient sample volume or improper application. This transparency reduces the ambiguity that plagues some lateral flow devices where internal workings are hidden. Sensitivity and specificity have been validated through WHO malaria RDT evaluation programs using panels of wild and cultured parasites. The test detects parasitemia levels above 100 parasites per microliter of blood for both P. falciparum and P. vivax, which is clinically relevant for symptomatic infections requiring treatment. Specificity exceeds 99% when tested against cross-reactive conditions including dengue, leptospirosis, typhoid, and other febrile illnesses common in malaria-endemic areas. Shelf life is 24 to 30 months when stored at 4-30°C, which is critical for stockpiling in tropical climates where cold chain infrastructure is unreliable. The extended temperature stability means the test remains functional even when stored at ambient temperatures in resource-limited settings. Each kit contains individually sealed test devices, buffer vials, blood collection pipettes, and instructions for use. The test requires no special training beyond basic clinical skills and can be performed by nurses, paramedics, or trained community health workers. For distributors supplying national malaria control programs, public health departments, NGO field operations, and private diagnostic laboratories, Advantage PAN Malaria Card represents a WHO-evaluated rapid diagnostic platform with predictable consumption tied to malaria case loads. Sara Wellness has been exporting rapid diagnostic test kits and laboratory reagents from India for 15 years.

Acon Urine HCG Pregnancy Test Kit
Two lines or one. That's all a pregnancy test comes down to. But ask any pharmacist, clinic manager, or hospital procurement officer how much rides on those two little lines being reliably accurate — and the conversation gets more serious very quickly. Because a false result, in either direction, is not just a product failure. It's a human failure. The ACON urine hCG Pregnancy Test Kit is built on the understanding that reliability is non-negotiable. ACON Laboratories, headquartered in San Diego and one of the world's leading manufacturers of rapid diagnostic tests, uses a chromatographic immunoassay format that detects human chorionic gonadotropin — the pregnancy hormone — in urine at a sensitivity threshold of 25 mIU/mL. That's the level at which hCG is consistently detectable in clinically confirmed early pregnancies. The test is calibrated against the WHO International Standard (3rd edition) and has FDA clearance, two regulatory benchmarks that procurement managers across almost every market in the world recognise and accept as evidence of validated performance. The test works in three minutes. First morning urine is preferred for maximum accuracy, but the test can be performed at any point during the day. Each strip is individually foil-sealed, maintaining integrity until the moment of use. The result reads simply: two lines positive, one line negative, no line in the control window means the test is invalid and should be repeated. Nothing about the procedure requires training or lab equipment — which is precisely why this product moves so effectively across pharmacy chains, government health outreach programmes, antenatal clinics, and over-the-counter retail. For importers and distributors sourcing diagnostic rapid tests in volume, the ACON hCG strip kit offers the rare combination of brand recognition, regulatory compliance, and competitive unit economics. The 50-strip box format is the standard across institutional procurement — hospitals, clinics, and NGO supply chains all order in this configuration. Shelf life runs to 36 months from manufacture under standard storage between 2 and 30°C, which makes inventory planning straightforward even for markets with longer supply chains. Sara Wellness has been exporting diagnostic and lab supply products to buyers across Africa, the Middle East, and Southeast Asia for 15 years. Rapid test kits like the ACON hCG strip are among the highest-velocity SKUs in our catalogue. We understand volume pricing, documentation requirements for IVD products in different export markets, and the importance of consistent batch quality across repeated shipments. Reach out with your volume requirement and we will put together a quote worth looking at.