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Sigma-Aldrich

Goat Anti-Human IgG Antibody, Fc, Alkaline Phosphatase conjugate

Chemicon®, from goat

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.46

biological source

goat

Quality Level

conjugate

alkaline phosphatase conjugate

antibody form

affinity purified immunoglobulin

antibody product type

secondary antibodies

clone

polyclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable
western blot: suitable

isotype

IgG

shipped in

wet ice

target post-translational modification

unmodified

Related Categories

General description

Alkaline Phosphatase-conjugated Affinity Purified Goat anti-Human IgG
Immunoglobulin G (IgG), is one of the most abundant proteins in human serum with normal levels between 8-17 mg/mL in adult blood. IgG is important for our defense against microorganisms and the molecules are produced by B lymphocytes as a part of our adaptive immune response. The IgG molecule has two separate functions; to bind to the pathogen that elicited the response and to recruit other cells and molecules to destroy the antigen. The variability of the IgG pool is generated by somatic recombination and the number of specificities in an individual at a given time point is estimated to be 1011 variants.

Specificity

Based on immunoelectrophoresis, the antibody reacts with the heavy chain of human IgG but not with the light chains of most human immunoglobulins.. No antibody was detected against normal human IgM or IgA, or against non-immunoglobulin serum proteins, but the antibody may cross-react with immunoglobulins from other species.

Application

Goat anti-Human IgG Antibody, Fc, Alkaline Phosphatase conjugate detects level of Human IgG & has been published & validated for use in ELISA & WB.
Research Category
Secondary & Control Antibodies
Research Sub Category
Fragment Specific Secondary Antibodies
Western Blot:
1:5,000-1:50,000 dilution can be used.

Optimal working dilutions must be determined by the end user.

Quality

Routinely evaluated by Enzyme-linked Immunosorbent Assay.

ELISA:
1:5,000-1:50,000 dilution can be used.

Linkage

Replaces: MABN1055

Physical form

Goat secondary antibody IgG in Lyophilized Buffer containing 0.01 M Tris HCl, 0.25 M NaCl, pH 8.0 with 15 mg/mL BSA and 0.05% sodium azide.

RECONSTITUTION:
Reconstitute with sterile distilled water to match the volume indicated on the vial label. Centrifuge product if it is not completely clear after standing for 1-2 hours at room temperature.
Unpurified

Storage and Stability

Stable for 1 year at 2–8°C from date of receipt.
After reconstitution the product is stable for several weeks at 2–8°C as an undiluted liquid. After dilution do not use for more than one day. For extended storage after reconstitution, add an equal volume of glycerol (ACS grade for better) to make a final concentration of 50% glycerol followed by storage at -20°C in undiluted aliquots for up to 12 months. Please note the concentration of protein (and buffer salts) will decrease to one-half of the original after the addition of glycerol. Avoid repeated freeze/thaw cycles.

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.

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Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Aquatic Chronic 3

Storage Class Code

11 - Combustible Solids

WGK

WGK 3


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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LINGO-1, a transmembrane signaling protein, inhibits oligodendrocyte differentiation and myelination through intercellular self-interactions.
Jepson, S; Vought, B; Gross, CH; Gan, L; Austen, D; Frantz, JD; Zwahlen, J; Lowe et al.
The Journal of Biological Chemistry null

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