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AP113A

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

Biologische Quelle

goat

Qualitätsniveau

Konjugat

alkaline phosphatase conjugate

Antikörperform

affinity purified immunoglobulin

Antikörper-Produkttyp

secondary antibodies

Klon

polyclonal

Speziesreaktivität

human

Hersteller/Markenname

Chemicon®

Methode(n)

ELISA: suitable
western blot: suitable

Isotyp

IgG

Versandbedingung

wet ice

Posttranslationale Modifikation Target

unmodified

Allgemeine Beschreibung

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.

Spezifität

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.

Anwendung

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

Optimal working dilutions must be determined by the end user.

Qualität

Routinely evaluated by Enzyme-linked Immunosorbent Assay.

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

Verlinkung

Replaces: MABN1055

Physikalische Form

Unpurified
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.

Lagerung und Haltbarkeit

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.

Rechtliche Hinweise

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

Haftungsausschluss

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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Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3


Analysenzertifikate (COA)

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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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