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MAB397

Anti-Glutamate Receptor 2 Antibody, extracellular, clone 6C4

clone 6C4, Chemicon®, from mouse

Synonim(y):

GluR2

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Rozmiar/SKUDostępnośćCena netto
100 μg

Dostępne do wysyłki DZISIAJzKuehne + Nagel Sp. z o.o.

2710,00 zł

Informacje o tej pozycji

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
6C4, monoclonal
Application:
ELISA, ICC, IHC, IP, RIA, WB
Citations:
404

2710,00 zł


Dostępne do wysyłki DZISIAJSzczegóły


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biological source

mouse

Quality Segment

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

6C4, monoclonal

species reactivity

monkey

species reactivity (predicted by homology)

mouse, rat, canine

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable, immunocytochemistry: suitable, immunohistochemistry: suitable, immunoprecipitation (IP): suitable, radioimmunoassay: suitable, western blot: suitable

isotype

IgG2a

NCBI accession no.

UniProt accession no.

target post-translational modification

unmodified

Gene Information

dog ... Gria2(482667)
mouse ... Gria2(14800)
rat ... Gria2(29627)
rhesus monkey ... Gria2(574344)

General description

Glutamate receptors (GluRs) can be categorized as ionotropic or metabotropic and subcatergorized by their agonist preferences (NMDA, AMPA or Kainic acid). There are four types of AMPA selective GluR subunits (GluR1, GluR2, GluR3 and GluR4). Tetrameric or pentameric combinations of different subunits contributes to the functional diversity of AMPA receptors. In general, AMPA receptors mediate fast synaptic current at most excitatory synapses, with stoichiometry characterized by subtype composition. Although subunit composition of AMPA receptors varies, they must contain at least one edited GluR2 subunit to be calcium impermeable. The critical residue controlling calcium permeability is in the pore loop region. In GluR1, GluR3, and GluR4, this positionis occupied by a Gln residue. In GluR2, it is occupied by an Arg residue. It has been shown experimentally that the presence of Arg in this position blocks CA2+ ion permeability, while a Gln does not. Relative calcium permeability in AMPA receptor channels may be significant in pathological neurotoxic damage and long term changes in nervous system responses.
102 kDa

Application

Anti-Glutamate Receptor 2 Antibody, extracellular, clone 6C4 detects level of Glutamate Receptor 2 & has been published & validated for use in ELISA, IC, IH, IP, RIA & WB with more than 50 product citations.
Immunocytochemistry:
on 4% paraformaldehyde fixed cells was used in a previous lot:2-3 µg/mL (Vissavajjhala, 1996; Osten, 1998; Passafaro, 2001).

ELISA/RIA:
A previous lot of this antibody was used in ELISA/RIA.(Vissavajjhala, 1996).

Immunohistochemistry on 50 µm, 4% paraformaldehyde fixed brain sections: 1:500-1:800 (Vissavajjhala, 1996; Yung, 1998; Kumar; 2002).

Immunoprecipitation: 2-4 µg/mL (Osten, 1998).

Western blot: 1-2 µg/mL (Vissavajjhala, 1996; Osten, 1998); membrane preparations are suggested for enhanced signals.

Optimal working dilutions and protocols must be determined by end user.

Biochem/physiol Actions

Recognizes the large N-terminal extracellular domain of Glutamate Receptor 2 (GluR2). No cross-reactivity observed with other AMPA/Kainate GluR subunits. On western blots of brain extracts from rat, macaque monkey, and dog, MAB397 recognizes a band at approximately 102 kDa corresponding to full length GluR2. Other proteins noted by Western blot at 66 kDa or lower molecular weight appear to be breakdown products of GluR2 (Vissavajjhala, 1996). By immunohistochemistry GluR2 is widely distributed at both the cellular and synaptic levels. MAB397 recognizes GluR2 present in a vast majority of, but not all, GABAergic interneurons (Vissavajjhala, 1996).

Physical form

Format: Purified
Purified immunoglobulin from culture supernatant
Purified mouse immunoglobin IgG2a liquid in buffer containing PBS, no preservative.

Preparation Note

Stable for 6 months at -20ºC in undiluted aliquots from date of receipt.
Handling Recommendations: Upon receipt, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage the IgG2a and affect product performance.

Analysis Note

Control
Positive Control: Cerebral cortex and pyramidal neurons, mouse brain lysate.
Routinely evaluated by Western Blot on mouse brain lysates.

Western Blot Analysis:
1:1000 dilution of this lot detected glutamate receptor 2 on 10 μg of mouse brain lysates.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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AB10529ABN241MABN1189
description

clone 6C4, Chemicon®, from mouse

description

serum, from rabbit

description

from rabbit, purified by affinity chromatography

description

clone 14C12.2, from mouse

species reactivity

monkey

species reactivity

mouse, rat

species reactivity

human, mouse, rat

species reactivity

mouse, rat, human

Gene Information

dog ... Gria2(482667)
mouse ... Gria2(14800)
rat ... Gria2(29627)
rhesus monkey ... Gria2(574344)

Gene Information

human ... GRIA2(2891)

Gene Information

human ... GRIA1(2890)
mouse ... Gria1(14799)
rat ... Gria1(50592)

Gene Information

human ... GRIA2(2891)

biological source

mouse

biological source

rabbit

biological source

rabbit

biological source

mouse

clone

6C4, monoclonal

clone

polyclonal

clone

polyclonal

clone

14C12.2, monoclonal

antibody form

purified immunoglobulin

antibody form

serum

antibody form

affinity isolated antibody

antibody form

purified antibody

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated


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12 - Non Combustible Liquids

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WGK 2



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Questions

  1. Is it possible to use two primary antibodies from different species but of the same isotype for double staining Immunofluorescence? Specifically, considering MAB397 and GluR2.

    1 answer
    1. Yes, it is possible to use two primary antibodies from different species but of the same isotype for double staining Immunofluorescence. Specifically, for MAB397 and GluR2, one can use an anti-mouse and an anti-rabbit secondary antibody to distinguish reactivity of the primary antibodies.

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