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AB1074

Sigma-Aldrich

Anti-Influenza A Antibody

Chemicon®, from goat

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

goat

Quality Level

antibody form

purified immunoglobulin

clone

polyclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable
immunofluorescence: suitable
immunohistochemistry: suitable
western blot: suitable

shipped in

wet ice

Specificity

Specific for Influenza A by IHA. Recognizes H1N1 and H3N2 and probably other Flu A strains. Non reactive with HEp-2 cells. May react with chicken cellular proteins. Does not react with Influenza B, RSV, Parainfluenza 1/2/3 or Adenovirus.

Immunogen

Influenza A-USSR (H1N1).

Application

Anti-Influenza A Antibody is an antibody against Influenza A for use in ELISA, IF, IH & WB.
Applications include ELISA, fluorescence microscopy, immunoblotting; unboiled samples in 1mM DTT and 2% SDS only and immunohistochemistry. Final working dilutions must be determined by end user.

Titer: 1:1,000 by indirect immunofluorescence. (1:2,500 by hemagglutination inhibition.)
Research Category
Infectious Diseases
Research Sub Category
Infectious Diseases - Viral

Physical form

Format: Purified
Protein A Purified goat immunoglobulin in PBS (0.01 M, pH 7.2) with 0.1% sodium azide as a preservative.
Protein A purified

Storage and Stability

Maintain at +2–8°C for 3 months or at -20°C in aliquots for up to 12 months after date of receipt. Avoid repeated freeze/thaw cycles.

Analysis Note

Control
Influenza Control Slides, Catalogue Number 5010-5

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Amy Y Chang et al.
Respiratory research, 17(1), 62-62 (2016-05-25)
The hexapeptide SLIGRL-amide activates protease-activated receptor-2 (PAR-2) and mas-related G protein-coupled receptor C11 (MRGPRC11), both of which are known to be expressed on populations of sensory nerves. SLIGRL-amide has recently been reported to inhibit influenza A (IAV) infection in mice
Wataru Yamazaki et al.
Transboundary and emerging diseases, 66(1), 341-348 (2018-09-30)
Transboundary animal diseases, including highly pathogenic avian influenza, cause vast economic losses throughout the world. While it is important to identify the sources and propagation routes of the spread, such strategies are often hindered by incomplete epidemiological evidence. Isolation/detection of
Hao Chen et al.
Virology journal, 14(1), 242-242 (2017-12-24)
Numerous toxicological studies have focused on injury caused by exposure to single types of nanoparticles, but few have investigated how such exposures impact a host's immune response to pathogen challenge. Few studies have shown that nanoparticles can alter a host's
Mechanism of inactivation of influenza viruses by immobilized hydrophobic polycations.
Hsu, BB; Yinn Wong, S; Hammond, PT; Chen, J; Klibanov, AM
Proceedings of the National Academy of Sciences of the USA null
Xiang Xu et al.
PloS one, 11(10), e0164501-e0164501 (2016-10-08)
Host-derived proteases can augment or help to clear infections. This dichotomy is exemplified by cathepsin L (CTSL), which helps Hendra virus and SARS coronavirus to invade cells, but is essential for survival in mice with mycoplasma pneumonia. The present study

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