Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More

BD™ MAX™ GBS

BD MAX™ GBS is a fully-automated, real-time PCR method for the detection of GBS from enriched culture. It simplifies detection of GBS colonization in antepartum pregnant women, and rapidly identifies Group B Streptococcus after an overnight Lim Broth enrichment.

Supplier:  BD™ 441772

Catalog No. B441772


Add to Cart

Description

Description

The BD MAX™ GBS assay as implemented on the BD MAX System is a qualitative in vitro diagnostic test designed to detect Group B Streptococcus (GBS) DNA in Lim Broth cultures, after incubation for greater than or equal to (≥)18 hours, obtained from vaginal-rectal swab specimens from antepartum pregnant women. The test incorporates automated DNA extraction to isolate the target nucleic acid from the specimen and real-time polymerase chain reaction (PCR) to detect a 124 bp region of the cfb gene sequence of the Streptococcus agalactiae chromosome. Results from the BD MAX GBS assay can be used as an aid in determining colonization status in antepartum women.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

95%
Group B Streptococcus Testing
BD MAX™ GBS Extraction Tubes (24), BD MAX™ GBS Sample Buffer Tubes (24), BD MAX™ Septum Caps (25), BD MAX™ GBS Reagent Strips (24), BD MAX™ GBS Master Mix (24)
0.967
SDS
Documents

Documents

Product Certifications
Promotions

Promotions

Provide Content Correction

We continue to work to improve your shopping experience and your feedback regarding this content is very important to us. Please use the form below to provide feedback related to the content on this product.

Product Title

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.

Cancel Submit