[TQ1110] ExcelTaq™ 2X Q-PCR Master Mix (SYBR, ROX), 200 RXN

Description

Specifications

Clone	IHC583
Source	Mouse Monoclonal
Positive Control	Breast Carcinoma, Urothelial Carcinoma
Dilution Range	1:200

GATA3 is a transcription factor important in cell proliferation, development, and differentiation. GATA3 is mostly observed in breast and urothelial carcinomas, and rarely present in other cancers such as endometrial endometrioid adenocarcinoma. Among the breast carcinomas, GATA3 has a lower expression in luminal B subtype breast carcinoma. Studies have found GATA3 expression to be associated with ER (estrogen receptor), PR (progesterone receptor), and Her2 in breast cancer cases. Urothelial carcinomas stain positively for GATA3 in invasive or high grade tumors, therefore Anti-GATA3 is useful for carcinoma diagnosis when breast and bladder are plausible.

Name of Product

HAMA – Human Anti Mouse
Antibodies Detection Kit

Catalog Number

MQHM Z

Short Info

Lateral Flow Assay designed for the detection of Human Anti Mouse Antibodies (HAMA) in human serum.

This product is only available in the EU!

Method/Platform

Lateral Flow

Range/Assay Sensivity

97%

Test Principle

The HAMA Detection Kit is an immunoassay designed for qualitative determination of Human Anti Mouse Antibodies in human serum.

HAMA from patient’s sample bind first to mouse antibodies which are conjugated to gold nanoparticles.

In a second step the HAMA will be caught by mouse IgG antibodies, coated on the Test Line (T) of the nitrocellulose membrane.

In the presence of the HAMA-conjugat-complex  a band becomes visible at the location of the Test Line (T).

The surplus of gold particles continues to migrate through the membrane and is captured at the Control Line (C) by specific antibodies.

Color’s intensitiy of the test line is directly proportional to the HAMA concentration in the sample.

Brief Instructions

Storage

2-8°C

Components

HAMA Test Unit, Chase Buffer, Evaluation Cards

5 tests
Lateral Flow Assay designed for the detection of Human Anti Mouse Antibodies (HAMA) in human serum.

• Real time qPCR kit
• For screening Anatoxin gene cluster
• Use in combination with Attogene Algae DNA isolation kit

Description

Not all cyanobacterial strains produce toxins. However, the toxin-producing strains cannot be distinguished from the nontoxin-producing strains by traditional light microscopy, commonly
used to monitor water bodies.  An alternative for the differentiation of potentially toxic strains from nontoxic strains is to use molecular methods to detect the presence of toxin biosynthetic genes. Such methods are already available and could be used for the detection and identification of potential microcystin and nodularin producers present in environmental samples (Attogene catalog number NA2024).

Screening for the toxin itself, can be very costly.  In turn, real time PCR for the detection of the anaC gene in cyanobacterial strains and environmental samples can be a key indicator for the prescense of cyanobacteria capable of expressing the Anatoxin toxin.  Attogen has thus, designed primer pairs and probes targeting a the conserved anaC gene region in order to enable the amplification and detection of several producer genera using real time PCR.  Screening for the toxin genes can save significant costs and act as a triage for samples needing to be analyzed for the toxin itself.

Real time qPCR kit
For screening Anatoxin gene cluster
Use in combination with Attogene Algae DNA isolation kit