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Merck
CN

62533

Hybriscan™ D kit

Beer, suitable for food and beverages,microbiology and in situ hybriziation

Synonym(s):

Beer Spoilage Organisms HybriScan™D, FastScan Beer

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About This Item

UNSPSC Code:
41171621
NACRES:
NA.85

Key Documents

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Product Name

HybriScan™D Beer, suitable for microbiology

usage

sufficient for 96 reactions

manufacturer/tradename

(HybriScan™)

technique(s)

microbe id | in situ hybriziation: suitable

application(s)

food and beverages
microbiology

shipped in

wet ice

storage temp.

2-8°C

suitability

Megasphaera spp.
Lactobacillus spp.
Pediococcus spp.
Pneumococcus spp.

Quality Level

100

Related Categories

Features and Benefits

Sensitivity (after pre enrichment): 1-10 cfu/L

General description

HybriScan™ D kits detect and simultaneously identify microorganisms using rRNA as the detection target. The principle is based on in situ sandwich hybridization with two specific probes. As the rRNA of dead cells is degraded in the presence of RNase, only living cells are detected. Each cell has several thousand rRNA copies, so neither PCR nor a polymerase is needed for this technology, which means that this molecular biology test is not inhibited by the sample matrix, for example food, beverages and water. We recommend a 24-hour enrichment in NBB broth (Cat. No. 50725)

Legal Information

HybriScan is a trademark of ScanBec GmbH

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Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Carc. 1B - Eye Dam. 1 - Met. Corr. 1 - Muta. 2 - Resp. Sens. 1 - Skin Corr. 1A - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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A Mehling et al.
Regulatory toxicology and pharmacology : RTP, 108, 104473-104473 (2019-09-09)
In the last 20 years, alternative approaches to the identification of skin sensitisation hazards have been at the forefront of the 3Rs and have helped refine the validation and acceptance processes. However, experience with the local lymph node assay showed

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