Find Verified Superoxide Dismutase%28Sod%29 Assay Kit Suppliers, Manufacturers and Wholesalers

Perkin Elmer
RoboRack 175ul Conductive Filter Tips, Sterile
We offer sterile and non-sterile tips for a variety of dispenser channel sizes and volume requirements. Tips to support liquid transfers from multiple laboratory containers including test tubes, vials, troughs, deep-well plates and microplates (up to 384-well) are available as well. Our portfolio of consumables includes both cell-based and biochemical assay platforms, reagents and kits, as well as a complete range of high quality and application-focused microplates for your assay applications, detection technologies, or plate reader requirements. Our Conductive Aerosol Barrier RoboRack MPII disposable tips for use with MultiPROBE II VersaTip Plus adapters are available in popular sizes in standard format for conventional liquid sample processing, sterile, provide liquid level sensing, and are available in ten 96-tip RoboRacks per case.

Cat. No : 11FK45. SD BIOLINE Dengue Duo

(Dengue NS1 Ag + IgG/IgM)

The SD BIOLINE Dengue Duo kit is a rapid, an in-vitro immunochromatographic, one step assay designed to detect both dengue virus NS1 antigen and antibodies to Dengue virus (Dengue IgG/IgM) in human serum, plasma or whole blood. SD BIOLINE Dengue Duo rapid test contains two test devices (left side ; Dengue NS1 Ag test, right side ; Dengue IgG/IgM test). The SD BIOLINE Dengue Duo kit is intended only for an initial screening test and reactive samples should be confirmed by a supplemental assay such as RT-PCR, IgM / IgG ELISA or HI (Hemagglutination inhibition) test.

Detect Dengue Ag and Ab simultaneously at once.

Cover acute to convalescence stage

Performance: Sensitivity : 92.4% (Dengue NS1 Ag), 94.2% (Dengue IgG/IgM)

Specificity : 98.4%(Dengue NS1 Ag), 96.4% (Dengue IgG/IgM)

In primary infection with the dengue virus, IgG antibody appears a few days after IgM. In primary infections, IgG antibodies are produced at a lower level compared to IgM but will persist for many years after infection. In secondary infections, IgG response may rise quickly before or simultaneously with an IgM response and will become the predominant immunoglobulin isotype in secondary infections.

Product Details:
Number of Reactions(Preps)/Kit :96
Brand : Abbott
ICMR Approved ; Yes
Test Method : (SARS-CoV-2) RT-PCR
Cat. No : 09N77-095
The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria

Product Details:

Size 96 wells/Plate
Format Indirect
Incubation Time 30 + 30 + 5 + 10 + 1
Sample Type Serum
Storage 2-8 C
Cat No STGS-R
The Scrub Typhus Detectâ?¢ IgG ELISA test for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA assay system for the detection of IgG antibodies in human serum to OT-derived recombinant antigen. For research use only. Not for use in diagnostic procedures.

The complete kit includes one 96 well strippable plate with all necessary reagents and controls.

Made in Canada
Health Canada approved
CE Mark and ISO certified
The product has proven to have 100% Specificity and 96% Sensitivety

Stock availabity: 2 Million tests/kit in Canada
Production: up to 5 Million tests/kit weekly

The Rapid Response COVID-19 Antigen Rapid Test Device is an in vitro immunochromatographic assay for the direct and qualitative detection of SARS-CoV-2 viral nucleoprotein antigens from nasal and nasopharyngeal secretions from individuals suspected of COVID-19 within 6 days of symptom onset. This test is authorized for use at the Point of Care i.e., in patient care setting. Results are for the identification of SARS-CoV-2 viral nucleoprotein antigen. Antigen is generally detectable in nasopharyngeal and nasal secretions during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories are required to report all positive results to the appropriate public health authorities. Negative results should be treated as presumptive, and do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patientâ??s recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management. The Rapid Responseâ?¢ COVID-19 Antigen Rapid Test Device is for use at the Point of Care for professional use only.

PRODUCT INFORMATION:

Product: Rapid Respose
Sample: Nasal / Nasopharyngeal secretions
Format: Cassette
Quantity: 25 Tests/Kit per box
Time to result: 15 minutes
Storage Condition: 2-30 C/36-86 F
Test Principle: Immunochromatographic Assay

CONTENTS - Individually packed test devices
Extraction Buffer
Extraction tube
Nozzle with filter
Tube stand
Individually packed swabs
Package Insert

Product Details:
Number of Reactions(Preps)/Kit :96 Wells
Brand : InBios
Sample Material : Serum
Formet : Immunocapture
Incubation Time : 30+30+30+10
Cat. No : CHKG-C
CHIKjj Detect : IgG ELISA Kit
The CHIKjj DetectTM IgG ELISA is designed for the qualitative detection of IgG antibodies present in human serum targeting chikungunya virus E2/E1 proteins. This test is for the presumptive clinical laboratory diagnosis of chikungunya virus infection. This assay is intended for use only in patients with clinical symptoms consistent with chikungunya infection.

The complete kit includes one 96 well strippable plate with all necessary reagents and controls.

Key Features :

Developed using a novel technology1 that outperforms traditional antigen preparations, resulting in highly sensitive detection of recent and past CHIKV infection.
>90% Sensitivity and Specificity
DENV Detect and CHIKjj Detect can be run in parallel for differential diagnosis.
CE Marked
Ordering :

Cat No : CHKG-C
Formet : Immunocapture
Quantity : 96 wells/Plate
Incubation Time : 30 + 30 + 5 + 10 + 1
Sample Type : Serum
Storage : 2-8
Shelf Life : 12 months

Product Details:
Number of Reactions(Preps) per Kit : 100
Brand : Seegene
ICMR(Govt) Approved : Yes
Test Method : (SARS-CoV-2) RT-PCR
Test Time : 2 Hours
Cat. No : RP10243X
-Detection of COVID-19 specific target genes in a single tube- Reliable result with three target genes- Results within 1 hour and 50 minutes after extraction- Convenient workow on the automated MDx platform- Suitable for high-throughput- Providing whole process control for assay validity- Automated data interpretation with Seegene Viewer

Additional Information:
Delivery Time: Immediate

Product : O- Cresolphthalein Complexone
C.A.S. No. :2411-89-4
M.F. :C32H32N2 O12
M.W. :636.62gm/mole

Specifications:
Solubility 0.1% (0.1N NaOH) = Clear solution
Absorption maximum (0.1N NaOH) at ?max = 572-578nm
Absorptivity (A1%1cm in 0.1N NaOH, at ?max on dried substance) = >790
Loss On Drying (110�°C) = <6%

Product Description:

o-Cresolphthalein Complexone is complexometric reagent derived from o-Cresolphthalein. It shows violet-red color in alkaline media and is a principle compound for the determination of hardness of water.Also used as Calcium Assay Kit as direct colorimetric assay based on the O-Cresolphtalein (OCPC) method without deproteinization of the sample. The calcium determination is based on the reaction of calcium with O-Cresolphthalein complexone in alkaline solution, which yields a violet colored complex. The intensity of the color formed is proportional to the calcium concentration in the sample. Absorbance of the Ca2+-O-Cresolphtalein complex is measured at 570nm. Wavelength range of sensitivity: 560 ~ 590nm.

Product Details:

Brand J.Mithra
Test Kit Type HBsAg Test Kit (Rapid)
Detects All the 11 subtype of HBsAg
Sensitivity 100% by WHO Evaluation
Specificity 100% by PATH USA Evaluation
Cat. No HB010100
Intended Use : Hepacard is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV).

Salient Features:
Detects all the 11 subtype of HBsAg.
Antigen Sensitivity- 0.5 ng/ml.
No sample preparation required.
See through Device for easy result interpretation.
Shelf life-30 months at 2-30C.
WHO Evaluated with 100% Sensitivity.

Evaluations:

PATH USA: Sensitivity 100% and Specificity 100% .
DEPT. OF CLINICAL VIROLOGY, CMC VELLORE: Sensitivity 100% and Specificity 100%
Approved By Drug Controller General Of India( DCGI) For use In Blood Banks.

Product Details:
Brand : CTK BioTech
Samples : Serum
Storage : 2-8 C
Size : 96 Well
Cat. No. : E1025

The Total Thyroxine (T4) ELISA is a solid-phase enzyme-linked immunosorbent assay based on the principle of the competitive ELISA technique for quantitative determination of Thyroxine in human serum.

The three main kit components are:

1) Solid microwells pre-coated with anti-T4

2) T4 Calibrators

3) Liquid T4 Enzyme Conjugate Mixture comprised of T4 labelled with horseradish peroxidase (T4-HRP)

Product Freature:

Analytical Sensitivity: 176 aµg/dL at 2-SD
Specificity: No cross-reactivity or interference with
d-Thyroxine 10 aµg/mL
d-Triiodothyronine 100 aµg/mL
Iodotyrosine 100 aµg/mL
Diiodotyrosine 100 aµg/mL
TBG 50 aµg/mL
Human Albumin 50 aµg/mL
Phenylbutazone 25 aµg/mL
Phenytoin 50 aµg/mL
ASA 500 aµg/mL
Acetaminophen 500 aµg/mL
Accuracy: correlation coefficient 0.98 with a reference method
Intra Assay Precision: CV a?¤ 5.9%
Inter Assay Precision: CV a?¤ 7.6%
Product Specification :
Anti-T4 Ab Coated Microwells
Total T4 Calibrators:
C1 (0 ng/mL)
C2 (2.0 ng/mL)
C3 (5.0 ng/mL)
C4 (10.0 ng/mL)
C5 (15.0 ng/mL)
C6 (25.0 ng/mL)
Total T4 Assay Control
Total T4 Enzyme Concentrate
Enzyme Buffer
Wash Buffer Concentrate
TMB Substrate
Stop Solution
Product Insert

Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : Serum / Plasma
Storage : 2-8 C
Cat No : AE0315
The TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay for the qualitative detection of IgM anti- Chikungunya virus in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of acute infection with Chikungunya viruses. Any reactive specimen with the TRUSTwell CHIK IgM Test must be confirmed with alternative testing method(s) and clinical findings.

TEST PRINCIPLE:

TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay based on the principle of the indirect immunoassay technique for the detection of IgM anti- Chikungunya virus in human serum or plasma. The TRUSTwell CHIK IgM Test is composed of two key components: 1) Solid microwells pre-coated with recombinant CHIK antigen(s); 2) Liquid conjugates composed of monoclonal anti-human IgM reagent conjugated with horse reddish peroxidase (HRP-anti-Human IgM conjugates). During the assay, the test specimen is first incubated with the coated microwells. IgM anti- Chikungunya virus, if present in the specimen, binds to the antigen coated on the microwell surface.

In the second incubation with the HRP-anti Human IgM conjugates, the IgM antiChikungunya antibody absorbed on the surface of microwell reacts to the conjugates, forming a complexed conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm.

Clinical Performance:

A total of 336 specimens from susceptible subjects were tested by TRUSTwell CHIK IgM and by a commercial reference ELISA kits.

Relative Sensitivity: 91.3 %, (95 % CI: 73.2 % -97.6 %) Relative Specificity: 96.8 %, (95 % CI: 94.2 % -98.3 %) Overall Agreement: 96.4%, (95 % CI: 93.9 % -98.0 %).

Perkin Elmer
Automated Workstation Tips 900 ul Filter Tip, Clear
We offer sterile and non-sterile tips for a variety of dispenser channel sizes and volume requirements. Tips to support liquid transfers from multiple laboratory containers including test tubes, vials, troughs, deep-well plates, and microplates (up to 384-well) are available as well. Our portfolio of consumables includes both cell-based and biochemical assay platforms, reagents, and kits, as well as a complete range of high quality and application-focused microplates for your assay applications, detection technologies, or plate reader requirements. Our Clear MBP Tips for the Varispan Arm provide liquid level sensing and are available in ten 96-tip racks/case.
Specifications
Automation Compatible Yes
Color - Clear
Disposable Tip Types - clear, non-sterile
Pipetting Arms - Varispan
Product Brand Name - JANUS
Quantity in a Package Amount - 10.0 Units
Unit Size - 900 ul
Volume Capacity - 900 L

Product Details:
Number of Reactions(Preps)/Ki : 25T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits): 10-15 mins
CAT No : RK055-25
STANDARD Q COVID-19 Ag is a rapid Immunochromatographic assay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.

Qualitatively detects specific antigens to SARS-CoV-2 present in Human Nasopharynx.
The test should be used as an aid in early diagnosis of symptomatic cases in healthcare setting having ILI.
Validated by ICMR & AIIMS
Sensitivity of 84.38 % & Specificity of 100%
Sample Type- Human Nasopharyngeal swab (No other sample recommended)
Results in 15-30 mins

Product Details:

Brand Roche
Result Time (Rapid Kits) 15 min
CAT No : 11621947196
Qualitative detection of troponin in anticoagulated

(EDTA or heparin) venous whole blood

Reaction time: 15 min.

Positive result from a threshold (cut-off) of 100 ng/L

Storage at 2 to 8 C

Test can be used immediately after removal from the

refrigerator

Storage for 4 weeks at room temperature (15 to 25 C)

Roche TROP T sensitive rapid assay is available in 5

and 10 pack sizes

Content:

5 disposable test strips (individually sealed)

5 pipettes (150 L)

disposable labels

1 package insert

Product Name: Citric Acid Monohydrate

"Type: Food/Feed Additives
Origin: China
CAS No.: 5949-29-1
AUCO No.: 104
Packing: 25kg bag"

Items Standard
CHARACTERISTICS "COLORLESS OR
WHITE CRYSTAL"
IDENTIFICATION TEST PASS THE TEST
"CLARITY & COLOUR
OF SOLUTION" "20%WATER SOLUTION
CLARITY"
ASSAY 99.5%-101.0%
MOISTURE 7.5%-9.0%
SULPHATED ASH 0.1%
SULPHATE 150 ppm
OXALATE 350 ppm
CALCIUM 200 ppm
HEAVY METALS 10 ppm
IRON 50 ppm
CHLORIDE 50 ppm
"READILY CARBURETED
SUBSTANCE" "STANDARD
COLOUR"
BARIUM PASS THE TEST
BACTERIAL ENDOTOXIN 0.5 IU/mg
ALUMINIUM 0.2 ppm
ODOR ODORLESS
FILTRATION C-C

Cat. No. - PB102-01

Packing - 1kit+C5:C53

Price - 20580

Health benefits of Cashew nuts
Cashews are high in calories. 100 g of nuts provide 553 calories. They packed with soluble dietary fiber, vitamins, minerals and numerous health-promoting phytochemicals that help protect from diseases and cancers.

They are rich in heart-friendly monounsaturated fatty acids like oleic, and palmitoleic acids. These essential fatty acids help lower harmful LDL-cholesterol while increasing good HDL cholesterol in the blood. Research studies suggest that the Mediterranean diet which is rich in monounsaturated fatty acids contribute to preventing coronary artery disease and strokes by favoring healthy blood lipid profile.

Cashew nuts are abundant sources of essential minerals. Manganese, potassium, copper, iron, magnesium, zinc, and selenium are especially concentrated in them. A handful of cashew nuts a day in the diet would provide enough of these minerals and may help prevent deficiency diseases. Selenium is an important micronutrient, which functions as a co-factor for antioxidant enzymes such as Glutathione peroxidases, one of the most powerful antioxidants in the body. Copper is a cofactor for many vital enzymes, including cytochrome c-oxidase and superoxide dismutase (other minerals function as co-factors for this enzyme are manganese and zinc). Zinc is a co-factor for many enzymes that regulate growth and development, gonadal function, digestion, and DNA (nucleic acid) synthesis.

Principle Nutrient Value Percentage of RDA
Energy : 553 Kcal 28%
Carbohydrates : 30.19 g 23%
Protein : 18.22 g 32.5%
Total Fat 43.85 g 146%
Cholestero : 0 mg 0%
Dietary Fiber : 3.3 g 8.5%
Vitamins

Product Details:
Number of Reactions(Preps)/Kit ; 96 Wells
Brand : InBios
Format : Immunocapture
Specimen : Serum
Cat No : ZKM2-1
The ZIKV Detect 2.0 IgM Capture ELISA is intended for the qualitative detection of Zika virus IgM antibodies in human sera for the presumptive clinical laboratory diagnosis of Zika virus infection. The assay is intended for use only in patients with clinical signs and symptoms consistent with Zika virus infection, and/or CDC Zika virus epidemiological criteria (e.g., history of residence in or travel to a geographic region with active Zika transmission at the time of travel, or other epidemiological criteria for which Zika virus testing may be indicated). Assay results are for the presumptive detection of IgM antibodies to Zika virus (ZIKV). Positive results must be confirmed by following the latest CDC guidelines for the diagnosis of Zika virus infection.

Results of this test are intended to be used in conjunction with clinical observations, patient history, epidemiological information, and other laboratory evidence to make patient management decisions. Zika IgM levels are variable over the course of the infection and may be detectable near day four post onset of symptoms and persist up to approximately 12 weeks following initial infection.

Negative results may be seen in specimens collected before day four post onset of symptoms or after the window of detectable IgM closes, and therefore do not preclude the possibility of Zika virus infection, past or present.

1st Commercial serology kit to receive FDA Marketing Authorization
CE Marked
Differentiates Zika IgM positive patients from those infected with other flaviviruses such as West Nile or Dengue
Sensitivity: >90%
Specificity: >96%
Results in 4 hours
Tests up to 28 unknown specimens.

From as little as $1.00 FoB per test - including IFU in Language of your choice!
COVID Rapid Test / Lateral Flow
- SARS-CoV-2 Antigen Kit Self Test Kit
- Nasal Swab based
- Qualitative
- IVD (Invitro diagnostic medical device)
- Rapid immunochromatographic assay
- 12 Minutes to result
- Shelf Life 18 months
- EU common list approved.
- In use: BE, BG, CY, FR, RO, SI, ES
- Validation Completed:
- FR, DE, ES
UK DHSC Approved.
- Validation completed & In use
- Specificity 100.0%
- Sensitivity 93.0%

Certifications:

EU HSC Approved
UK DHSC Approved
(included in JRC database)
CE
Directive 98/79/EC
EN ISO 13485:2016
BS EN 13612:2002
ISO 14971:2019
EN ISO 23640:2015
ISO 15223-1:2016
EN ISO 18113-1:2011
EN ISO 18113-4:2011
EN 62366-1:2015

More Information is available at our website.
Please contact us directly, visit our website, follow us on LinkedIn and/or Instagram.
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in = fiigureofficial

Intended use

The helicobacter-pylori antigen rapid test kit (stool) is a rapid visual immunoassay for the qualitative detection of helicobacter pylori antigen in human stool specimens. This kit is used as an aid in the diagnosis of h. Pylori infection.



Introduction

Helicobacter pylori (also known as campylobacter pylori) as a spiral-shaped gram negative bacteria which infects the gastric mucosa. H. Pylori to causes several gastro-enteric diseases such as non-ulcerous dyspepsia, gastric and duodenal ulcer, active gastritis and can even increase the risk of stomach adenocarcinoma.

The epidemiologic study shows that more than 50% of the world's population is infected by h. Pylori strains. Infection is more prevalent in developing countries. The lowest infection rate is 20%, and the highest infection rate can be 90% in developing countries. H. Pylori strains is the major reason to cause chronic gastritis and gastric ulcers, 80%-90% chronic gastritis patients and 95%-100% gastric ulcers patients are infected by h. Pylori strains. So the detection and treatment of h. Pylori strains infection is very important.

At present several invasive and non-invasive approaches are available to detect this infection state. Invasive methodologies require endoscopy of the gastric mucosa with histologic, cultural and urease investigation, which are expensive and require some time for diagnosis. Alternatively, non-invasive methods are available such as breath tests, which are extremely complicated and not highly selective, and classical elisa and immunoblot assays. This kit belongs to non-invasive approach.