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WHAWB120306

QIAcard Indicating FTA Cards

classic, 4 sample areas per card, pkg of 25 cards

Synonym(s):

QIAcard FTA Indicating Classic (25), Whatman FTA, Z747491

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About This Item

UNSPSC Code:
41105500
NACRES:
NB.22

To inquire about this product WHAWB120306, please contact your local Merck office or dealer. Contact Technical Service

description

Indicating FTA Classic Card with 4 sample areas per card, 125 μl maximum volume/sample area, 500 μl maximum total volume/card

manufacturer/tradename

Qiagen WB120306

packaging

pkg of 25 cards

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This Item
BAF371090020BAF371090030BAF371090031
packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea

material

octagonal red PTFE-coated

material

octagonal yellow PTFE-coated

material

octagonal blue PTFE-coated

material

octagonal red PTFE-coated

manufacturer/tradename

Bel-Art F37109-0034

manufacturer/tradename

Bel-Art F37109-0020

manufacturer/tradename

Bel-Art F37109-0030

manufacturer/tradename

Bel-Art F37109-0031

L × diam.

12.7 in. × 3.2 in.

L × diam.

1.5 in. (38.1 mm) × 0.3125 in. (8 mm)

L × diam.

2 in. (50.8 mm) × 0.3125 in. (8 mm)

L × diam.

3 in. (76.2 mm) × 0.5 in. (12.7 mm)

General description

FTA Cards offer a compact room-temperature storage system that reduces the need for precious freezer space.

QIAcard FTA classic format with 4 spot area to collect, stabilize, process, transport, and archive colored samples such as blood. FTA technology enables cell lysis on contact, denatures proteins and immediate stabilization and protection of nucleic acids.

FTA classic cards utilize QIAcard FTA technology that simplifies the handling and processing of nucleic acids. FTA Cards contain chemicals that lyse cells, denature proteins and protect nucleic acids from nucleases, oxidation and UV damage. FTA cards rapidly inactivate organisms, including blood-borne pathogens, and prevent the growth of bacteria and other microorganisms.

Convenient for protocols that require different locations for testing and archiving samples. Different samples can be processed independently.

Features and Benefits

  • Includes a pink dye that turns white when a colorless sample is applied.
  • 4 sample areas for application of up to 500 μl sample volume per card.
  • Simply apply your sample to the FTA Card. Cell membranes and organelles are lysed and the released nucleic acids are entrapped in the fibers of the matrix. The nucleic acids remain immobilized and are preserved for transport, immediate processing or long-term room temperature storage.
  • Since captured nucleic acids are preserved, FTA Cards facilitate sample collection in remote locations and simplify sample transport.
  • Ship your samples back to the laboratory without expensive special handling or dry ice and process at your convenience.
  • FTA Cards can be used with virtually any sample type: Blood, Cultured cells, Buccal cells, Plasmids, and Solid tissue.
  • Captured nucleic acids are ready for purification when you are. Just take a punch from the FTA Card, wash with FTA Purification Reagent and rinse with TE-1 (10 mM Tris-HCI, 0.1 mM EDTA, pH 8) buffer. DNA on the washed punch is ready to use in applications such as PCR, SNP analysis, and real-time PCR. Since PCR products remain in solution, the punch can be used for multiple amplifications.

Other Notes

Sample integrity is optimized when FTA Cards are stored in a Multi-Barrier Pouch with a Desiccant Packet.
Field of Use : For internal research use only

Legal Information

FTA is a trademark of Qiagen Group
QIAcard is a trademark of Qiagen Group

Regulatory Information

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    G F Mazzuoli et al.
    Calcified tissue international, 38(1), 3-8 (1986-01-01)
    In this paper we present the results of a 12-month double-blind clinical multicenter study assessing the effects of synthetic salmon calcitonin (CT) administration in a group of white postmenopausal osteoporotic women. Treated patients were given 100 MRC units of synthetic
    Effects of salmon calcitonin and calcitonin gene related peptide (CGRP) on gastric mucosal barrier in stress induced rats.
    Z Kanay
    African Journal of Biotechnology, 8 (2009)
    K A Kelly et al.
    Endocrinology, 139(4), 2092-2101 (1998-04-07)
    Stromal cells are required for in vitro osteoclast differentiation and maturation. The murine bone marrow stromally derived BMS2 cell line exhibits adipocytic and osteoblastic features as well as the ability to support lymphopoiesis and myelopoiesis. This work examined the ability
    Mona M A Abdel-Mottaleb et al.
    International journal of pharmaceutics, 515(1-2), 384-389 (2016-11-05)
    Recently, a selective preferential accumulation of polymeric nanoparticles (in the size range around 100nm) has been observed in the follicular system of dermatitis skin. The present investigation aimed at clearly investigating the effect of irritant contact dermatitis on the barrier
    E Patois et al.
    European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 81(2), 392-398 (2012-03-17)
    Ultraviolet Resonance Raman (UVRR) spectroscopy with excitation at 244 nm was investigated here as a possible useful tool for fast characterization of biopharmaceuticals. Studies were performed on three protein drugs: salmon calcitonin (sCT), starch-peptide conjugate, and transforming growth factor-β3 (TGF-β3)

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