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Millipore

Hybriscan I kit

Candida albicans, suitable for clinical testing, environmental, food and beverages, microbiology and in situ hybriziation

Synonym(s):

Candida albicans HybriScanI, FastScan Candida albicans

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About This Item

UNSPSC Code:
41171621
NACRES:
NA.85
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Product Name

HybriScan I Candida albicans, suitable for microbiology

manufacturer/tradename

(HybriScan)

Quality Level

technique(s)

microbe id | in situ hybriziation: suitable

application(s)

clinical testing
environmental
food and beverages

microbiology

storage temp.

2-8°C

suitability

Candida albicans

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1 of 4

This Item
Z137294Z137316Z422878
disc diam.

40 mm

disc diam.

20 mm

disc diam.

80 mm

disc diam.

40 mm

capacity

60 mL

capacity

15 mL

capacity

350 mL

capacity

60 mL

manufacturer/tradename

Ace Glass 719046

manufacturer/tradename

Ace Glass 719040

manufacturer/tradename

Ace Glass 719050

manufacturer/tradename

Aldrich

pore size

70-100 μm porosity

pore size

70-100 μm porosity

pore size

70-100 μm porosity

pore size

-

description

joint I.D. 40 mm

description

joint I.D. 20 mm

description

joint I.D. 40 mm

description

-

General description

HybriScan I kits are intended for the identification and result confirmation of microorganisms using rRNA as the detection target. Several customers also use it to detect microorganisms in food, beverage and water samples. 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.

Features and Benefits

  • Sensitivity (cfu/assay): 1000

Legal Information

HybriScan is a trademark of ScanBec GmbH

Signal Word

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 Code

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


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Devon L Johnstone et al.
Brain : a journal of neurology, 142(3), 542-559 (2019-01-23)
Biallelic pathogenic variants in PLPBP (formerly called PROSC) have recently been shown to cause a novel form of vitamin B6-dependent epilepsy, the pathophysiological basis of which is poorly understood. When left untreated, the disease can progress to status epilepticus and
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Oncogenesis, 10(2), 18-18 (2021-02-28)
Mitochondrial proteases are key components in mitochondrial stress responses that maintain proteostasis and mitochondrial integrity in harsh environmental conditions, which leads to the acquisition of aggressive phenotypes, including chemoresistance and metastasis. However, the molecular mechanisms and exact role of mitochondrial
Michael E Pacold et al.
Nature chemical biology, 12(6), 452-458 (2016-04-26)
Serine is both a proteinogenic amino acid and the source of one-carbon units essential for de novo purine and deoxythymidine synthesis. In the canonical pathway of glucose-derived serine synthesis, Homo sapiens phosphoglycerate dehydrogenase (PHGDH) catalyzes the first, rate-limiting step. Genetic
Sha Yao et al.
Translational lung cancer research, 10(6), 2523-2538 (2021-07-24)
Lung cancer remains the major cause of cancer related death worldwide. The discovery of targeted therapies against activating mutations in genes like EGFR considerably improved the prognosis for a subgroup of patients but still leaves a large part without a
Scott J Hebbring et al.
Journal of neurochemistry, 120(6), 881-890 (2012-01-10)
Serine hydroxymethyltransferase (SHMT) catalyzes the transfer of a β-carbon from serine to tetrahydrofolate to form glycine and 5,10-methylene-tetrahydrofolate. This reaction plays an important role in neurotransmitter synthesis and metabolism. We set out to resequence SHMT1 and SHMT2, followed by functional

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