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IC REG LIN 3.3V 250MA SOT-223-3
Output Configuration: Positive
Output Type: Fixed
Number of Regulators:1
Voltage - Input (Max):16V
Voltage - Output (Min/Fixed):3.3V
Current - Output:250mA
Current - Quiescent (Iq):5 �µA
PSRR:44dB (100Hz)
Operating Temperature: -40�°C ~ 125�°C
Package:SOT-223-3

CY8C58LP Microcontroller IC 32-Bit Single-Core 80MHz 256KB (256K x 8) FLASH 100-TQFP (14x14)
Core Processor: ARM Cortex-M3
Core Size: 32-Bit Single-Core
Speed:80MHz
Number of I/O: 62
Program Memory Type: FLASH
Operating Temperature: -40C ~ 85C (TA)
Package / Case:100-LQFP

FERRITE BEAD 330 OHM 0402 1LN
330 Ohms @ 100 MHz 1 Power Line Ferrite Bead 0402 (1005 Metric) 800mA 220mOhm
Manufacturer Product Number
BKP1005EM331-T
Manufacturer: Taiyo Yuden
Part Status: Obsolete
Impedance @ Frequency: 330 Ohms @ 100 MHz
Current Rating: (Max)800mA
DC Resistance (DCR) (Max): 220mOhm
Operating Temperature: -55C ~ 85C
Package / Case:0402 (1005 Metric)
Size / Dimension:0.039" L x 0.020" W (1.00mm x 0.50mm)

Digital to Analog Converters - DAC QUAD 16-BIT +/-15V DAC
Resolution: 16 bit
Sampling Rate: 1.26 MS/s
Number of Channels: 4 Channel
Settling Time: 8 us
Output Type: Voltage
Interface Type: 3-Wire
Analog Supply Voltage: +/- 11.4 V to +/- 16.5 V
Digital Supply Voltage: 2.7 V to 5.25 V
Minimum Operating Temperature: - 40 C
Maximum Operating Temperature: + 85 C
Package / Case: TQFP-32
Number of Converters: 4 Converter
Pd - Power Dissipation: 381 mW
FPG:250PCS
Supply Voltage - Max: 16.5 V
Supply Voltage - Min: 11.4 V
Subcategory: Data Converter ICs

Type: HART Modems
Operating Supply Current: 179 uA
Minimum Operating Temperature: - 40 C
Maximum Operating Temperature: + 125 C
Mounting Style: SMD/SMT
Package / Case: LFCSP-24
Brand: ADI
Length: 4 mm
Packaging: Reel
Moisture Sensitive: Yes
Product Type: Interface - Specialized
FPQ:1500

Manufacturer: Panasonic
Product Category: Low Signal Relays - PCB
Packaging: Tube
Product: Low Profile Relays
Type: Miniature
Coil Voltage: 5 VDC
Relay Contact Form: 2 Form C (DPDT-NO, NC)
Contact Rating: 2A
Contact Current Rating: 2A
Maximum Switching Current: 2A
Coil Current: 40 mA
Coil Type: Non-Latching
Power Consumption: 200 mW
Contact Termination: Solder Pin
Coil Resistance: 125 Ohms
Contact Form: DPDT (2 Form C)

Converters - ADC Octal CH 12B 100MSPS Hi-SNR & Lo-Pwr ADC A 595-ADS5295PFP

SENSOR OPTICAL 10-150CM ANALOG

RF Connectors / Coaxial Connectors RA JACK PCB (Socket)
Mounting Style: Through Hole
Packaging: Tray
Body Material: Zinc Alloy
Body Finish: Nickel
Brand: Molex
Frequency: 18 GHz

As for Urine Reagent Analysis Strip Uncut Sheets , we have various parameters ranging from 1 to 12 .

We can provide you strip and uncut sheet URS format with high quality and competitive price

PRINCIPLE AND EXPECTED VALUES
URS Ascorbic acid: This test involves decolorization of Tillmann's reagent. The presence of ascorbic acid causes the color of the test field to change from blue-green to orange. Glucose: This test is based on the enzymatic reaction that occurs between glucose oxidase, peroxidase and chromogen. Glucose if first oxidized to produce gluconic acid and hydrogen peroxide in the presence of glucose oxidase. The hydrogen peroxide reacts with potassium iodide chromogen in the presence of peroxidase. The extent to which the chromogen is oxidized determines the color which is produced, ranging from green to brown. Low amounts of glucose are normally excreted in urine.3 Glucose concentrations as low as 100 mg/dL, read at either 10 or 30 seconds, may be considered abnormal if results are consistent. At 10 seconds, results should be interpreted qualitatively. For semi-quantitative results, read at 30 seconds only.


URS Bilirubin: This test is based on azo-coupling reaction of bilirubin with diazotized dichloroaniline in a strongly acidic medium. Varying bilirubin levels will produce a pinkish-tan color proportional to its concentration in urine. In normal urine, no bilirubin is detectable by even the most sensitive methods. Even trace amounts of bilirubin require further investigation. Atypical results (colors different from the negative or positive color blocks shown on the color chart) may indicate that bilirubin-derived bile pigments are present in the urine specimen, and are possibly masking the bilirubin reaction.

INTENDED USE

The test kit utilize purified Chlamydia Trachomatis Antibody antigen, based on GIFA principle and use indirect method to detect Urea Plasma Urealyticum antibody in human serum.


TEST PROCEDURE

1. Remove the test kit and put it at room temperature (for about 20-30mins) before testing.

2. Add 1 drop of Wash Buffer into the hole and allow the liquid soak the membrane completely.

3. Add 150l of the serum specimen into the hole and allow it to sufficient absorption.

4. Add 3 drops of Colloidal Conjugate into the hole and allow it to sufficient absorption.

5. Add 3 drops of Wash Buffer into the hole and allow it to sufficient absorption. Read the results within 3 minutes.

STORAGE
The kit can be stored at room temperature (2-30C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.

INTENDED USE

Feline Panleucopenia Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Panleucopenia Virus (FPV Ag) in cat's feces or vomit.

PRINCIPLE OF THE ASSAY

Feline Panleucopenia Virus(FPV) Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Panleucopenia Virus antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Panleucopenia Virus antigen in the sample.

INTERPRETATION OF RESULTS

Positive: The presence of both C band and T band, no matter T band is clear or vague.

Negative: Only clear C band appears.

Invalid: No colored band appears in C zone, no matter whether T band appears.

STORAGE

The kit can be stored at room temperature (2-30�°C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.

INTENDED USE

Feline Immunodeficiency Virus Ab Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Immunodeficiency Virus antibody (FIV Ab) in cat's blood.

PRINCIPLE OF THE ASSAY

Feline Immunodeficiency Virus Ab Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody in the sample.

INTERPRETATION OF RESULTS

Positive: The presence of both C band and T band, no matter T band is clear or vague.

Negative: Only clear C band appears.

Invalid: No colored band appears in C zone, no matter whether T band appears.

STORAGE

The kit can be stored at room temperature (2-30C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.

1. INTENDED USE

FIV Ab + FeLV Ag Combined Rapid Test is a combined cassette to differentially diagnose the presence of Feline Immunodeficiency antibody and Feline Leukemia Virus antigen in cat's blood.

Assay Time: 10-15 min

Sample: serum, plasma or whole blood

2. PRINCIPLE OF THE ASSAY

FIV Ab + FeLV Ag Combined Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has two testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody or FeLV antigen in the sample, a visible T band will appear in the corresponding testing window. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody or FeLV antigen in the sample.

3. KIT COMPONENT

- 10 foil pouches, each containing a cassette,pipette and desiccant

- 10 assay buffer tubes (0.5 mL each)

- 10 centrifugal tubes

- Product Manual

One Step Influenza A Test is a rapid qualitative assay that detects influenza type A (including the subtype H1N1) nucleoprotein antigen extracted from the nasal swab specimen. The device is used to aid in the diagnosis of influenza type A infection.

For in vitro diagnostic use only. For professional use only.

Influenza A SUMMARY

Influenza (commonly known as flu) is a highly contagious, acute viral infection of the respiratory tract. It is a communicable disease that is easily transmitted through the coughing and sneezing of aerosolized droplets containing live virus. Influenza outbreaks occur each year during the autumn and winter months. There are three types of influenza viruses: A, B, and C. Only influenza A viruses are further classified by subtype on the basis of the two main surface glycoproteins hemagglutinin (HA) and neuraminidase (NA). Influenza A subtypes and B viruses are further classified by strains.

Humans can be infected with influenza types A, B, and C viruses. Subtypes of influenza A that are currently circulating among people worldwide include H1N1, H1N2, and H3N2 viruses. Influenza B viruses can cause morbidity and mortality among humans, but in general are associated with less severe epidemics than influenza A viruses. Although influenza type B viruses can cause human epidemics, they have not caused pandemics. Influenza type C viruses cause mild illness in humans and do not cause epidemics or pandemics.

Influenza A PRINCIPLE

One Step Influenza A Test is a rapid immunochromatographic test for the visual detection of influenza type A antigen (nucleoprotein) extracted from the nasal swab specimen. The test adopts double antibody sandwich method.

When the extracted specimen is added into the test device, the specimen is absorbed into the device by capillary action, mixes with antibody-dye conjugate, and flows across the membrane pre-coated with influenza type A monoclonal antibody.

When the influenza type A antigen levels are at or above the target cutoff (the detection limit of the test), type A antigen in the specimen binds to the specific antibody-dye conjugate and are captured by influenza type A monoclonal antibody immobilized in the relative site of test region T of the device. This produces a colored test band in the test region. When the influenza type A antigen levels are zero or below the target cut off, there is not a visible colored band in the test region of the device. This indicates a negative result for influenza type A.

Intended Use

The One Step HAV IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Hepatitis A Virus (HAV) in Whole Blood /Serum / Plasma to aid in the diagnosis of Hepatitis A Virus.

Summary

Hepatitis A is an acute, usually self-limiting disease of the liver caused by hepatitis A virus (HAV). HAV is transmitted from person to person, primarily by the faecal-oral route. The incidence of hepatitis A is closely related to socioeconomic development, and seroepidemiological studies show that prevalence of anti-HAV antibodies in the general population varies from 15% to close to 100% in different parts of the world. One step HAV IgG/IgM Test is a simple, visual qualitative test that detects Hepatitis A Virus antibodies in human Whole Blood /Serum / Plasma. The test is based on immunochromatography and can give a result within 15 minutes.

Principle

The One Step HAV IgG/IgM Test is a qualitative membrane strip based immunoassay for the detection of Hepatitis A Virus antibodies (IgG and IgM) in Whole Blood /Serum / Plasma. The test device consists of: 1) a burgundy colored conjugate pad containing HAV recombinant envelope antigens conjugated with Colloid gold (HAV conjugates) and rabbit IgG-gold conjugates,2) a nitrocellulose membrane strip containing two test bands (T1 and T2 bands) and a control band (C band). The T1 band is pre-coated with the antibody for the detection of IgM anti-HAV, T2 band is coated with antibody for the detection of IgG anti-HAV, and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the test cassette, the specimen migrates by capillary action across the cassette. IgG anti-HAV, if present in the specimen, will bind to the HAV conjugates. The immunocomplex is then captured by the reagent pre-coated on the T2 band, forming a burgundy colored T2 band, indicating a HAV IgG positive test result and suggesting a recent or repeat infection. IgM anti-HAV if present in the specimen will bind to the HAV conjugates. The immunocomplex is then captured by the reagent coated on the T1 band, forming a burgundy colored T1 band, indicating a HAV IgM positive test result and suggesting a fresh infection. Absence of any T bands (T1 and T2) suggests a negative result. The test contains an internal control (C band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the T bands. Otherwise, the test result is invalid and the specimen must be retested with another device.

Storage and Stability

Store as packaged in the sealed pouch at room temperature or refrigerated (4-30 or 40-86). The test device is stable through the expiration date printed on the sealed pouch.
The test must remain in the sealed pouch until use.