All Products

Configuration: A/B/AB/D/D/Ctl/N/N
Technique: Detect A(ABO1), B(ABO2), D(RH1) antigens and possible anti-A and/or anti-B antibodies. Rh(D) and Weak D/Partial D antigens are detected with specific antibodies in Dvı- and Dvı+ microtubes.

Configuration: A/B/AB/D/CDE/Ctl/N/N
Technique: Detect A(ABO1), B(ABO2), Rh antigens and possible anti-A and/or anti-B antibodies. In Rh grouping, the presence of C and E antigens as well as Rh(D) antigens are detected.

Configuration: A/B/AB/D/CDE/Ctl/N/N
Technique: Detect A(ABO1), B(ABO2), Rh antigens and possible anti-A and/or anti-B antibodies. In Rh grouping, the presence of C and E antigens as well as Rh(D) and Weak D / Partial D antigens are detected.

Configuration: A/B/AB/D/Kell/Ctl/N/N
Technique: Detect A(ABO1), B(ABO2), RH(D) and Kell antigens and possible anti-A and/or anti-B antibodies.

Configuration: A/B/AB/D/Kell/Ctl/N/N
Technique: Detect A(ABO1), B(ABO2), RH(D), Weak D / Partial D antigens and Kell antigens and possible anti-A and/or anti-B antibodies.

Configuration: A/B/D/Ctl/A/B/D/Ctl
Technique: Detect A(ABO1), B(ABO2), RH(D), and Weak D / Partial D antigens.

Configuration: A/B/D/Ctl/A/B/D/Ctl
Technique: Detect A(ABO1), B(ABO2) and RH(D) antigens.

Configuration: A/B/AB/A1/H/Ctl/N/N
Technique: Detect A(ABO1), B(ABO2), A1(Lectin) and H antigens and possible anti-A and/or anti-B antibodies.

Configuration: AHG/AHG/AHG/AHG/AHG/AHG/AHG/AHG
Technique: This test is used to study polyspecific direct coombs, antibody screening and identification, cross match in coombs reagent medium, autocontrol and weak D tests.

Configuration: N/N/N/N/AHG/AHG/AHG/AHG
Technique: Antibody screening and identification and cross match tests by enzymatic and coombs method.

Configuration: N/N/N/N/N/N/N/N
Technique: Cross match, autocontrol, antibody screening and identification and determination of reverse ABO group with enzymatic technique.

Configuration: IgG/IgG/IgG/IgG/IgG/IgG/IgG/IgG
Technique: Study monospecific direct coombs, antibody screening and identification, cross match in IgG reactive media, autocontrol and weak D tests.

Configuration: AHG/AHG/AHG/AHG/AHG/AHG/AHG/AHG
Technique: This test is used to study polyspecific direct coombs, antibody screening and identification, cross match in coombs reagent medium, autocontrol and weak D tests.

Configuration: A/B/D/Ctl/N/N/AHG/AHG
Technique: Confirmation of blood groups of ABO and Rh(D) systems, compatibility tests, cross match tests with enzymatic and Coombs techniques and autocontrol test.

Configuration: N/N/N/N/AHG/AHG/AHG/AHG
Technique: Antibody screening and identification and cross match tests by enzymatic and coombs method.

Configuration: A/B/D/AHG/A/B/D/AHG
Technique: Perform ABO/Rh (D) blood group control of the patient and donor simultaneously, major/minor cross match tests and autoantibody test in Coombs environments on a single card.

Configuration: AHG/IgG/C3d/Ctl/AHG/IgG/C3d/Ctl
Technique: Detect red blood cells sensitized in vivo with IgG type immunoglobulins or complement C3d fractions.

Configuration: AHG/IgG/IgM/IgA/C3c/C3b/C4/Ctl
Technique: Investigation of the C3c, C3d and C4 components of the complement system, as well as IgA and IgM antibodies, facilitates rapid and accurate diagnosis in Direct Coombs negative cases.

Configuration: A/B/AB/D/D/Ctl/IgG/AHG
Technique: Detect A(ABO1), B(ABO2), D(RH1) antigens in newborns and perform a direct Coombs test.

Configuration: D/C/E/c/e/Cw/Kell/Ctl
Technique: Detect Rh and Kell antigens.

Configuration: C/E/c/e/C/E/c/e
Technique: Detect C(Rh2), E(Rh3), c(Rh4) and e(Rh5) antigens.

Configuration: D/Ctl/D/Ctl/D/Ctl/D/Ctl
Technique: Detect , RH(D), and Weak D / Partial D antigens.

Configuration: Kell/Ctl/Kell/Ctl/Kell/Ctl/Kell/Ctl
Technique: Detect Kell antigens.

Preparation of the erythrocyte suspension to be used in Across Gel cards.

Preparation of the erythrocyte suspension to be used in Across Gel cards.

Probe washing of “in vitro” diagnostic devices

Screening/identification of antibodies, autoantibody tests and cross-match tests by enzymatic method.

Screening/identification of antibodies, autoantibody tests and cross-match tests by enzymatic method.

Screening/identification of antibodies, autoantibody tests and cross-match tests by enzymatic method.

Detection of the presence of anti-A and/or anti-B isoagglutinins in serum/plasma

Detection of the presence of anti-A and/or anti-B isoagglutinins in serum/plasma

• Serial pipetting allows 50μL x 8, 25μL x 16 ve 10μL x 40 dispensing
• Disposable pipette tips

• Fast and reliable usage
• Compatible with 100 ml or 500 ml vials
 

• Across Gel® card area
• 500, 100 and 25 ml solution area
• RBC bottle area
• Suspension preparation tube area

• 200 Across Gel® card loading areas
• 6 x 16 sample loading areas
• 12 RBC loading areas
• 4 x 100 ml Across LISS and/or Bromelin area
• 3 96-well dilution plates area
• Incubator with a capacity of 24 Across Gel® cards
• Centrifuge with a capacity of 24 Across Gel® cards
• Waste container

• 100 Across Gel® card loading areas
• 3 x 24 sample loading areas
• 2 x 12 RBC loading areas
• 3 x 96 disposable pipette tips minimizing the risk of contamination
• 2 x 100 ml Across LISS and/or Bromeline area
• 1 x 96-well dilution plate area
• Incubator with a capacity of 12 Across Gel® cards
• Centrifuge with 12 Across Gel® card capacity                                             
• Second centrifuge option                                              
• Waste container 

• 24 Across Gel Card capacity.
• Acceleration, deceleration and time optimized for Across Gel Cards.
• Visual and audible alarm in case of unbalanced loading, power failure or at the end of processing time.
• Remaining processing time and centrifuge speed are shown on the digital display.
•Removable and replaceable rotor and card slots

• 24 Across Gel® Card capacity
• Two different blocks with 12 Across Gel® Card capacity each working independently.
• Previously adjusted at 37 ºC for Across Gel® Cards and time calibrated.
• Remaining processing time and temperature are shown on the digital display designed for two different blocks.
• Visual and audible alarm in case of power failure or at the end of processing time.
 

Screening of antibodies that may be clinically important in serum or plasma to be tested in anti-human globulin (AHG) media

Screening of antibodies that may be clinically important in the serum or plasma to be tested in an enzyme medium

Screening of antibodies that may be clinically important in serum or plasma to be tested in anti-human globulin (AHG) media

Screening of antibodies that may be clinically important in the serum or plasma to be tested in an enzyme medium

Screening of antibodies that may be clinically important in serum or plasma to be tested in anti-human globulin (AHG) media

Screening of antibodies that may be clinically important in the serum or plasma to be tested in an enzyme medium

Identification of clinically important antibodies in the serum or plasma to be tested in the presence of anti-human globulin (AHG)

Identification of antibodies that may be clinically important in the serum or plasma to be tested in enzyme media

Screening for antibodies that may be clinically important in the serum or plasma 

Control of Coombs tests with red blood cells sensitized with anti-D.

ABO / Rh (D) grouping is used in extensive quality control by detecting Rh phenotype, K antigen and screening irregular antibodies. Internal controls have to be performed regularly according to the local and national regulations. When test results come out as expected, it means that test procedures are performed correctly and, reagents and equipments produce correct results. When unexpected results are observed, patient test results have to be stopped and the source of error can be tracked.

Allo / Auto antibodies adsorbed to red cells in vivo or in vitro can be recovered by elution by separation. Eluate can then be used to identify a single antibody in multispecific serum, to indicate the presence of a weak antigen, to identify the antibody responsible for a positive direct antiglobulin test in the resulting hemolytic anemia or transfusion reaction, to identify antibodies causing hemolytic disease for newborn, or to prepare specific antibodies from serums that include unwanted antibodies.

Daratumumab (DARA) is an anti-CD38 monoclonal antibody which has promising results in relapsed and refractory multiple myeloma. DARA interferes with blood compatibility testing by causing panagglutination in the Indirect Antiglobulin Test and Cross-Match. Across Dara Remove can over come anti-CD38 antibody interference in one simple step. It inhibits the agglutination effect of Daratumumab thus preventing the false-positive reaction in Cross-Match and Indirect Agglutination Tests. Across Dara Remove Kit block s the CD38 molecule on the surface of the RBC. When treating RBC with Across Dara Remove, RBC behaves as if no Daratumumab was present in the patient’s sample.

• Custom operating system
• Touch screen
• Ability to detect agglutinations in microtubes over the original image of Across Gel® cards, thanks to its CCD camera.
• Thanks to its software; Automatic interpretation by detecting card and test type from barcodes of Across Gel® cards
• Ability to transfer the Across Gel® card image to the automation system along with the test results.
• Bidirectional communication

The principle of the Across Gel Brucella Coombs test is based on the detection of agglutination induced reactions resulting from the binding of IgG and IgM antibodies against B. abortus, B. melitensis and B. suis in patient serum samples and colored antigens in Brucella Antigenic Solution in Coombs medium by gel centrifugation technique.
Advantages
1. Can be used easily and safely in laboratories with ready-to-use products.
2. Ease of interpretation by gel centrifugation method.
3. Safer results with minimal risk of contamination.
4. Standardization.
5. Suitable for automation. Across System Card Reader allows you to send the results to the automated LIS system and record the test results. You can perform tests with Across Auto Systems without any intervention.
6. Screening or Titration result in 30 minutes.

Hydatid cyst is an important parasitic disease that threatens human and animal health and is very common in our country.
Serological diagnosis of hydatidosis; It is based on the principle of detecting samples containing anti-Echinococcus antibodies. Echinococcus Granulosis chimeric antigen is coated on sheep erythrocytes and detection is achieved by agglutinating these
erythrocytes with specific antibodies in the serum. Results against three different epitopes are seen in one microtube. It can be used easily and safely in almost all laboratories, including primary care laboratories. Thanks to itsease of standardization, it contributes to the reduction of application errors and is suitable for automation.

Löwenstein Medium and Löwenstein-Jensen (LJ) Medium are used for the isolation and culture of mycobacteria and this medium is a selective, differential and enriched medium for mycobacteria.
LJ Medium is an inspired egg-based medium developed from a modification of Jensen's Löwenstein formula.

Across Bio Myco is a decontamination and concentration kit. It is used in the processing of samples for the detection and production
of mycobacteria by microscopy, culture and molecular methods. For general laboratory use.
Across Bio Myco contains all the necessary materials for the easy and safe application of Sodium Hydroxide - N-acetyl-L-cysteine
decontamination and concentration method.
This method is recommended for liquefaction of samples such as sputum, precipitation of mycobacteria, selective killing of other
microorganisms, and thus more effective detection of mycobacteria in clinical samples. Across Bio Myco offers all the necessary
materials for the procedure in a set for each sample separately. Thus, by preventing cross and general contamination, it provides a
significant time and effort increase. In addition, Across Bio Myco has been designed to ensure that biohazardous materials are
disposed of safely. Across Bio Myco is an important aid in the detection of mycobacteria. However, it is not a tool used alone for the
diagnosis of mycobacteria.

Across Myco %2 Decontamination and Concentration Kit REF:520020

Across Myco %3 Decontamination and Concentration Kit REF: 520030

Across Myco %4 Decontamination and Concentration Kit REF: 520040