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Product details

H1N1 TaqMan RT-PCR Kit Dx

Catalog number DxTM27900

Price for DxTM27900

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Size / count 24 Reactions

About this product

Detection kits for H1N1 CE-IVDD marked in accordance with the European Commission Directive 98/79/EC. Research version available Available in TaqMan format for analysis Influenza is caused by three immunologic types of RNA viruses (A, B and C) within the Orthomyxoviridae family. Seasonal influenza is typically caused by three major subtypes of hemaglutinin (H1, H2 and H3) and two subtypes of neuraminidase (N1 and N2) . A novel sub-type of influenza A virus called pandemic H1N1 2009 virus was identified in Mexico and reported by the CDC and WHO in April, 2009 (Novel swine-origin influenza A (H1N1) virus investigation team, 2009; CDC, 2009; and Fraser et al., 2009) . H1N1 2009 is a novel sub-type virus that transmits easily between humans with 21 countries reporting cases within a month of initial identification (CDC, 2009-b) . It is essential that public health laboratories around the world undertake detailed surveillance to monitor the spread and impact of pandemic H1N1 2009 virus as well as try to predict future changes in virulence (Fraser et al., 2009) . Methods for the rapid diagnosis, case identification and tracking of this novel pathogen in the human population are therefore required to develop appropriate management strategies to mitigate morbidity and mortality. H1N1 TaqMan RT-PCR Kit, 24 reactions Ready to use format, including Master Mix for the target and PCR control to monitor for PCR inhibition and validate the quality Specific Primer and Probe mix for the pathogen/virus/viroid of interest Primer and Probe mix Positive and negative control to confirm the integrity of the kit reagents

Specifications

Catalog number
DxTM27900
Size / count
24 Reactions
Dry ice
Yes
Hazardous
Yes
Discontinued
No
MOQ
1
UNSPSC
41106313
UN Code
UN1845
Dot Regulated
True
Weight
30
Length
13
Shipping Conditions
Dry Ice
Storage Conditions
Freezer
Storage Temperature
-20
Width
15
Height
12
Shelf Life
All reagents can be used until the expiration date specified on their labels.

Frequently Asked Questions

What is the catalog number for H1N1 TaqMan RT-PCR Kit Dx?

The catalog number for H1N1 TaqMan RT-PCR Kit Dx is DxTM27900.

What sizes are available for H1N1 TaqMan RT-PCR Kit Dx?

H1N1 TaqMan RT-PCR Kit Dx is available in the following size(s): 24 Reactions.

Is H1N1 TaqMan RT-PCR Kit Dx in stock?

H1N1 TaqMan RT-PCR Kit Dx is currently made to order / not held in immediate stock. Contact us for lead time.

Are there any special shipping requirements for H1N1 TaqMan RT-PCR Kit Dx?

H1N1 TaqMan RT-PCR Kit Dx is classified as hazardous (additional shipping fees may apply) and requires dry ice shipping.

Where can I find the safety data sheet (SDS/MSDS) for H1N1 TaqMan RT-PCR Kit Dx?

The safety data sheet for H1N1 TaqMan RT-PCR Kit Dx is available here: https://norgenbiotek.com/sites/default/files/resources/DxTM27900%20-%20H1N1%20TaqMan%20RT-PCR%20Detection%20Kit%20Dx.pdf.

What is H1N1 TaqMan RT-PCR Kit Dx used for?

Detection kits for H1N1 CE-IVDD marked in accordance with the European Commission Directive 98/79/EC. Research version available Available in TaqMan format for analysis Influenza is caused by three immunologic types of RNA viruses (A, B and C) within the Orthomyxoviridae family. Seasonal influenza i

Do you provide a Certificate of Analysis (CoA) for this product?

A Certificate of Analysis is available for most products upon request. Contact our support team with the lot number to obtain the relevant CoA.

Is this product suitable for live cell imaging?

Suitability for live cell imaging depends on the specific reagent and conjugate used. Check the datasheet for imaging-specific validation, or contact us for guidance.

Is this product covered by a money-back guarantee?

Yes, we guarantee a full refund or store credit if this product arrives damaged beyond usability, or has a genuine performance issue under proper usage and storage, provided you report it immediately with evidence. Claims after the expiration date or due to improper storage after receipt are excluded.

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