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A4937

Sigma-Aldrich

Anti-Mouse IgA (α-chain specific)−Alkaline Phosphatase antibody produced in goat

affinity isolated antibody, buffered aqueous glycerol solution

Synonym(s):

Goat Anti-Mouse IgA (α-chain specific)−AP

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.46

biological source

goat

conjugate

alkaline phosphatase conjugate

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

buffered aqueous glycerol solution

technique(s)

direct ELISA: 1:30,000
western blot: 1:30,000

shipped in

wet ice

storage temp.

2-8°C

target post-translational modification

unmodified

Related Categories

General description

Immunoglobulin A (IgA) is the major mammalian antibody isotype that is synthesized in the gut associated lymphoid tissues. This immunoglobulin isotype modulates intestinal microorganisms and has been implicated in the pathogenesis of IgA nephropathy. Anti-Mouse IgA (α-chain specific)-Alkaline Phosphatase antibody is specific for mouse IgA when tested against purified mouse IgA, IgG, and IgM myeloma proteins.

Immunogen

Purified mouse IgA

Application

E. coli lysates and purified pili were analyzed by western blot using alkaline phosphatase conjugated goat anti-mouse IgA antibody as a secondary.
Anti-Mouse IgA (α-chain specific)-Alkaline Phosphatase antibody is suitable for use in ELISA. The product can also be used for western blot (1:30,000).

Physical form

Solution in 0.05 M Tris, pH 8.0, containing 1 mM MgCl2, 10 mM glycine, 1% bovine serum albumin, 50% glycerol and 15 mM sodium azide.

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.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Duncan B Sutherland et al.
Current opinion in immunology, 24(3), 261-268 (2012-04-17)
Immunoglobulin A (IgA) is the most abundantly produced antibody isotype in mammals. The primary function of IgA is to maintain homeostasis at mucosal surfaces. IgA is generated in specialized gut associated lymphoid tissues (GALT) by T cell-dependent and T cell-independent
Finn Terje Hegge et al.
Proceedings of the National Academy of Sciences of the United States of America, 101(29), 10798-10803 (2004-07-14)
Several major bacterial pathogens and related commensal species colonizing the human mucosa express phosphocholine (PC) at their cell surfaces. PC appears to impact host-microbe biology by serving as a ligand for both C-reactive protein and the receptor for platelet-activating factor.
Young Youl Hyun et al.
Cell transplantation, 21(11), 2425-2439 (2012-04-25)
T-cell dysregulation plays an important role in the pathogenesis of immunoglobulin A nephropathy (IgAN). Adipose-derived stem cells (ASCs) have been reported to be able to prevent tissue damage through immune-modulating effects. To evaluate the effects of ASCs in high IgA
Rachel Chikwamba et al.
Transgenic research, 11(5), 479-493 (2002-11-20)
We have produced a functional heat labile enterotoxin (LT-) B subunit of Escherichia coli in maize. LT-B is a multimeric protein that presents an ideal model for an edible vaccine, displaying stability in the gut and inducing mucosal and systemic
J S Sandhu et al.
Transgenic research, 9(2), 127-135 (2000-08-22)
Respiratory syncytial virus (RSV) is one of the most important pathogens of infancy and early childhood. Here a fruit-based edible subunit vaccine against RSV was developed by expressing the RSV fusion (F) protein gene in transgenic tomato plants. The F-gene

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