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A3673

Anti-Mouse IgG (γ-chain specific)−Peroxidase antibody produced in goat

affinity isolated antibody, buffered aqueous solution

Synonyme(s) :

Goat Anti-Mouse IgG (γ-chain specific)−HRP

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A propos de cet article

UNSPSC Code:
12352203
NACRES:
NA.46
MDL number:
Conjugate:
peroxidase conjugate
Clone:
polyclonal
Application:
ELISA (d)
Citations:
85
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biological source

goat

Quality Level

conjugate

peroxidase conjugate

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

mouse

technique(s)

direct ELISA: 1:15,000

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

General description

Immunoglobulin G (IgG) is a glycoprotein antibody that regulates immune responses such as phagocytosis and is also involved in the development of autoimmune diseases. Mouse IgGs have four distinct isotypes, namely, IgG1, IgG2a, IgG2b, and IgG3. IgG1 regulates complement fixation in mice.
Goat Anti-Mouse IgG (γ-chain specific)-Peroxidase antibody is specific for mouse IgG when tested against purified mouse IgA, IgG, and IgM myeloma proteins.

Immunogen

purified mouse IgG

Application

Goat Anti-Mouse IgG (γ-chain specific)-Peroxidase antibody has been used for ELISA applications at a dilution of 1:3000.
HRP conjugated goat anti-mouse gamma chain specific was used to detect neutralizing antibodies against HIV1 in sera and mucosal washings by ELISA. 3′3′5,5 tetramethylbenzidine (Sigma) was used as the substrate for development.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin with preservative.

Preparation Note

Prepared using the periodate method described by Wilson, M.B., and Nakane, P.K., in Immunofluorescence and Related Staining Techniques, Elsevier/North Holland Biomedical Press, Amsterdam, p215 (1978).

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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Cet article
A6029A0420A3187
biological source

goat

biological source

goat

biological source

goat

biological source

goat

species reactivity

mouse

species reactivity

human

species reactivity

human

species reactivity

human

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

technique(s)

direct ELISA: 1:15,000

technique(s)

direct ELISA: 1:10,000

technique(s)

direct ELISA: 1:50,000, dot blot: 1:100,000 (chemiluminescent), immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:200

technique(s)

direct ELISA: 1:30,000, immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:50, western blot: 1:30,000

conjugate

peroxidase conjugate

conjugate

peroxidase conjugate

conjugate

peroxidase conjugate

conjugate

alkaline phosphatase conjugate

clone

polyclonal

clone

polyclonal

clone

polyclonal

clone

polyclonal


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pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Classe de stockage

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Contenu apparenté


Basil Rapoport et al.
Journal of immunology (Baltimore, Md. : 1950), 197(12), 4560-4568 (2016-12-04)
Graves' hyperthyroidism, a common autoimmune disease caused by pathogenic autoantibodies to the thyrotropin (TSH) receptor (TSHR), can be treated but not cured. This single autoantigenic target makes Graves' disease a prime candidate for Ag-specific immunotherapy. Previously, in an induced mouse
C Acquaviva et al.
Oncogene, 20(51), 7563-7572 (2001-12-26)
c-Fos proto-oncoprotein is rapidly and transiently expressed in cells undergoing the G(0)-to-S phase transition in response to stimulation for growth by serum. Under these conditions, the rapid decay of the protein occurring after induction is accounted for by efficient recognition
Chad P Grabner et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 35(38), 13133-13147 (2015-09-25)
Night blindness can result from impaired photoreceptor function and a subset of cases have been linked to dysfunction of Cav1.4 calcium channels and in turn compromised synaptic transmission. Here, we show that active zone proteins RIM1/2 are important regulators of



Numéro d'article de commerce international

RéférenceGTIN
A3673-1ML04061833367773
A3673-.25ML04061835805037
A3673-.5ML04061835805044

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