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F8264

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

affinity isolated antibody, buffered aqueous solution

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ConditionnementRéférenceDisponibilitéPrix
1 mL
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552,00 €
469,20 €

A propos de cet article

UNSPSC Code:
12352203
NACRES:
NA.46
MDL number:
Conjugate:
FITC conjugate
Clone:
polyclonal
Application:
IF (d)
Citations:
15

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biological source

goat

Quality Level

conjugate

FITC conjugate

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

buffered aqueous solution

technique(s)

direct immunofluorescence: 1:64

storage temp.

2-8°C

target post-translational modification

unmodified

General description

IgG antibody subtype is the most abundant serum immunoglobulins of the immune system. It is secreted by B cells and is found in blood and extracellular fluids and provides protection from infections caused by bacteria, fungi and viruses. Maternal IgG is transferred to fetus through the placenta that is vital for immune defence of the neonate against infections. Anti-Mouse IgG (γ-chain specific)-FITC antibody is specific for is specific for mouse IgG when tested against purified mouse IgA, IgG (all subclasses), and mouse IgM. Goat anti-mouse IgG is isolated by affinity isolation and conjugated to Fluorescein Isothiocyanate (FITC), isomer I.

Immunogen

Purified mouse IgG

Application

Anti-Mouse IgG (γ-chain specific)-FITC antibody may be used for immunofluorescence of mouse spleen cells at a working antibody dilution of 1:64. For ELISA using mice sera, antibody dilution of 1:50 was used. The antibody was also used in anti-nucear antibody detection using mouse sera and for labeling Saimiri brain endothelial cells for exhaustive photon reassignment microscopy
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunofluorescence (1 paper)

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin 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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Cet article
F8646F9384F4018
conjugate

FITC conjugate

conjugate

FITC conjugate

conjugate

FITC conjugate

conjugate

FITC conjugate

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

biological source

goat

biological source

goat

biological source

goat

biological source

goat

technique(s)

direct immunofluorescence: 1:64

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:320

technique(s)

direct immunofluorescence: 1:16

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:200, indirect immunofluorescence: 1:64

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

form

buffered aqueous solution

form

buffered aqueous solution

form

buffered aqueous solution

form

buffered aqueous solution


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Classe de stockage

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)



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Contenu apparenté


C M Shih et al.
Journal of clinical microbiology, 34(9), 2297-2299 (1996-09-01)
We determined whether the span of infectivity of Lyme disease spirochetes (Borrelia burgdorferi) to vector ticks varies with the mode of infection in laboratory mice. Noninfected larval deer ticks were permitted to feed on two strains of spirochete-infected mice that
C M Shih et al.
Journal of clinical microbiology, 33(12), 3164-3168 (1995-12-01)
We determined whether the infectivity of the Lyme disease spirochete (Borrelia burgdorferi) to vector ticks varies with the duration of infection in laboratory mice. Thus, noninfected nymphal deer ticks were permitted to feed on two strains of early (2 months
B Pouvelle et al.
Molecular medicine (Cambridge, Mass.), 3(8), 508-518 (1997-08-01)
Chondroitin-4-sulfate (CSA) was recently described as a Plasmodium falciparum cytoadherence receptor present on Saimiri brain microvascular and human lung endothelial cells. To specifically study chondroitin-4-sulfate-mediated cytoadherence, a parasite population was selected through panning of the Palo-Alto (FUP) 1 P. falciparum



Numéro d'article de commerce international

RéférenceGTIN
F8264-2ML04061833620472
F8264-1ML04061838354549

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