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@berserk

17 Hours ago

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@berserk

17 Hours ago

Aenean vulputate eleifend tellus. Aenean leo ligula, porttitor eu, consequat vitae, eleifend ac, enim. Aliquam lorem ante, dapibus in, viverra

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@berserk

17 Hours ago

Aenean vulputate eleifend tellus. Aenean leo ligula, porttitor eu, consequat vitae, eleifend ac, enim. Aliquam lorem ante, dapibus in, viverra

T4

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Immunoenzymatic colorimetric method for quantitative determination of thyroxine (T4) concentration in human serum and plasma. T4 ELISA kit is intended for laboratory use only.

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ANA 12 Line Dot
ANA 12 Line Dot
  • ANA 12 LINE is used for the separate qualitative determination of auto-antibodies to nuclear and cytoplasmic antigens (dsDNA, nucleosomes, Sm, ribosomes, histones, RNP, SS-A 60 kDa, SS-A 52 kDA, SS-B, Scl-70, CENP-B and Jo-1) in human serum or plasma.
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p-aNCA Plus
p-aNCA Plus
  • pANCA IFA is used for the sensitive qualitative and semiquantitative determination of IgG antibodies to neutrophil cytoplasmatic antigens (ANCA) in human serum using indirect immunoflorescence assay on formalin fixed human granulocytes for the differential diagnosis of systemic vasculitis (SV). The assay is used for the confirmation of pANCA positive results found on ethanol fixed granulocytes.
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Anti Musk Ab
Anti Musk Ab
  • Anti-MuSK IFA is a reagent set for the qualitative and semi-quantitative measurement of antibodies against the MuSK antigen in human serum. For this HEp-2 cells, which have been transfected with MuSK antigens.
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Anti Transglutaminase (TTG) IgA
Anti Transglutaminase (TTG) IgA
  • Anti-huTransG is used for the quantitative or semi-quantitative determination of IgA autoantibodies to tissue transglutaminase (tTG, transglutaminase 2) in human serum or plasma for the differential diagnosis of celiac disease.
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COXSACKIE B5 RNA Ctrl
COXSACKIE B5 RNA Ctrl
  • Coxsackieviruses are nonenveloped, icosahedral, single stranded RNA (+) viruses of small size (28-30 nm) included in the genus Enterovirus. Enteroviruses are responsible for a wide array of clinical diseases, including aseptic meningitis, encephalitis, myocarditis and pericarditis, respiratory disease or hand-foot-and-mouth disease.
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Dengue IgG
Dengue IgG
  • Dengue (DF) and dengue hemorrhagic fever (DHF) are caused by one of four closely related, but antigenically distinct, virus serotypes (DEN-1, DEN-2, DEN-3, and DEN-4), of the genus Flavivirus. DF and DHF are primarily diseases of tropical and sub tropical areas, and the four different dengue serotypes are maintained in a cycle that involves humans and the Aedes mosquito. Infections produce a spectrum of clinical illness ranging from a nonspecific viral syndrome to severe and fatal hemorrhagic disease. Clinical manifestations include rash, sudden onset of fever, chills, severe headache, nausea, myalgias and arthralgias, leukopenia, thrombocytopenia and hemorrhagic manifestations. It occasionally produces shock and hemorrhage, leading to death. Important risk factors for DHF include the strain of the infecting virus, as well as the age, and especially the prior dengue infection history of the patient. Dengue viraemia appears to be universal in febrile patients with dengue; it occurs prior to the onset of fever and symptoms and peaks 2–3 days after the onset of illness. A diagnosis of acute infection with dengue virus can be made by isolating the virus or by detecting viral genome or antigen. Serologically, a primary infection with dengue virus results in detectable levels of IgM antibodies by the third afebrile day after infection. These IgM antibodies persist for 1–2 months after infection. IgG antibodies are detected approximately 14 days after onset of primary infections. Secondary infections with dengue virus are characterized by a rapid increase in IgG antibody levels. Owing to the relatively late increase in antibody levels to a concentration that can be detected diagnostically, a negative result for an antibody test early in the course of disease is not definitive. Specimens should be collected at least 7 days after the onset of symptoms in order to rule out the possibility of an acute infection with dengue virus. Serology is the most widely applied method used in routine diagnosis. Traditionally, hemagglutination inhibition and virus neutralization tests have been used. At present ELISAs for IgM and IgG antibodies are the standards for the serological analysis of dengue virus infections, as they are simple and allow large numbers of samples to be tested.
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Mumps IgG/IgM
Mumps IgG/IgM
  • Mump virus is the ethiological agent of the mump. Mumps is an illness characterized by parotid swelling and usually accompanied by generalized symptoms. It is one of the most common causes of aseptic meningitis. Other common symptoms are orchitis and inflammation of pancreas and ovaries. Some of the mumps infections are subclinical or unrecognized and may require viral isolation and/or some other serological procedure. Current methods for serodiagnosis of mumps infection are serum neutralization, hemagglutination-inhibition, immunofluorescence, complement fixation and ELISA tests. ELISA is as sensitive as the neutralization test and more sensitive than hemagglutination-inhibition and complement fixation. An increase in IgG titer is helpful, specially if can be shown to be greater than that against any parainfluenza virus. The IgM response is also useful, althouhg it may be suppressed in cases that occur after prior sensibilization. It can also be falsely positive as a result of concurrent parainfluenza virus infection.
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TOXOPLASMA GONDII DNA Ctrl
TOXOPLASMA GONDII DNA Ctrl
  • Toxoplasma gondii is a protozoan that presents three stages in its developmental life cycle: oocyst, tachyzoite and bradyzoite. While only members of the family Felidae can be definitive hosts of the parasite, a great variety of animals can harbour the tissue cysts. Although consuming contaminated food is the most common way of becoming infected, transplacental infection may occur. The disease is normally benign, but central nervous system disease may appear in immunocompromised patients and the newborn.
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SHBG
SHBG
  • Direct immunoenzymatic colorimetric method for quantitative determination of SHBG concentration in human serum or plasma. SHBG kit is intended for laboratory use only.
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Brucella IgG
Brucella IgG
  • Direct agglutination, Rose Bengal test, Coombs´test and ELISA are the most widely used techniques for the serologic diagnosis of brucellosis. Detection of IgG against Brucella lipopolysaccharide (LPS) is suitable for the diagnosis of all forms of the disease. The ELISA technique is sensitive and specific for the detection of IgG antibodies against Brucella.
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Autoimmune Hepatitis4(HepAK Dot)
Autoimmune Hepatitis4(HepAK Dot)
  • HepAK Dot is used for the qualitative determination of IgG autoantibodies to M2, LKM1, LC1 and SLA in human serum or plasma in for the differential diagnosis of autoimmune liver diseases.
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AMPLIRUN® VIBRIO CHOLERAE DNA CONTROL
AMPLIRUN® VIBRIO CHOLERAE DNA CONTROL
  • Vibrio cholerae is a Gram-negative, comma-shaped, flagellate, facultative anaerobic bacterium. Its natural habit is aquatic, frequently associated with zooplancton, shellfish or aquatic plants. Cholera disease is caused by toxigenic strains of serogroups O1 and O139. People are infected by drinking water or eating food contaminated with the cholera bacterium. The infection is often mild or without symptoms, but sometimes it can be severe, with watery diarrhea and vomiting that can lead to rapid dehydration and electrolyte imbalance.