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A5420

Sigma-Aldrich

Anti-Goat IgG (whole molecule)–Peroxidase antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

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Synonym(s):
Anti Goat Igg, Anti-Goat IgG (whole molecule)–Peroxidase antibody produced in rabbit
MDL number:
NACRES:
NA.46

biological source

rabbit

Quality Level

conjugate

peroxidase conjugate

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

goat

technique(s)

direct ELISA: 1:40,000
dot blot: 1:80,000-1:160,000
immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:200

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

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General description

Immunoglobulin G (IgG) belongs to the immunoglobulin family and is a widely expressed serum antibody. An immunoglobulin has two heavy chain and two light chain connected by disulfide bond. It is a glycoprotein and a major class of immunoglobulin. Goat IgG has two subclasses- IgG1 and IgG2.
Goat IgGs against target proteins are often used as primary antibodies in various research applications. Thus, secondary anti-goat IgGs conjugated to a detectable substrate are useful tools for the analysis of target proteins. Rabbit anti-goat IgG (whole molecule)-peroxidase antibody binds to all goat Igs.

Specificity

Specificity of Anti-Goat IgG- Peroxidase is determined by immunoelectrophoresis (IEP) versus normal goat serum and goat IgG.

Immunogen

Purified goat IgG

Application

LNCAP cell lysates were analyzed by western blot using HRP conjugated rabbit anti-goat IgG as the secondary at a 1:7500 dilution in TBSt for 1 hour at room temperature.
Rabbit Anti-Goat IgG (whole molecule)-Peroxidase antibody has been used for immunoblotting assays. The antibody can also be used for direct ELISA (1:40,000), dot blot (1:80,000-1:160,000) and immunohistochemistry (1:200) assays.
Anti-Goat IgG (whole molecule)–Peroxidase antibody has been used in
  • western blotting
  • immunohistochemical and immunofluorescent analysis
  • visualization of cross-reactivity
  • protein analysis
  • indirect ELISA for detection of specific IgG against C. pseudotuberculosis
  • immunoprecipitation (IP)

Biochem/physiol Actions

Immunoglobulin G (IgG) glycoprotein antibodies modulates several immune responses. It mainly participates in hypersensitivity type II and type III.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 0.05% MIT

Storage and Stability

For continuous use, store at 2-8 °C for up to one month. For extended storage, the solution may be frozen in working aliquots. Repeated freezing and thawing, or storage in "frost-free" freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use.

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Skin Sens. 1

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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The mammalian neuroendocrine hormone norepinephrine supplies iron for bacterial growth in the presence of transferrin or lactoferrin.
Freestone P P, et al.
Journal of Bacteriology, 182(21), 6091-6098 (2000)
Properdin plays a protective role in polymicrobial septic peritonitis.
Stover C M, et al.
Journal of Immunology, 180(5), 3313-3318 (2008)
Respiratory syncytial virus nonstructural proteins decrease levels of multiple members of the cellular interferon pathways.
Swedan S, et al.
Journal of Virology, 83(19), 9682-9693 (2009)
Suppression of thrombospondin 1 and 2 production by herpes simplex virus 1 infection in cultured keratocytes.
Choudhary A, et al.
Molecular Vision, 11, 163-168 (2005)
The stalk domain and the glycosylation status of the activating natural killer cell receptor NKp30 are important for ligand binding.
Hartmann J, et al.
The Journal of Biological Chemistry, jbc-M111 (2012)

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