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Merck
CN

G0545

Anti-GABAA Receptor (γ2 subunit) (extracellular) antibody produced in rabbit

affinity isolated antibody, lyophilized powder

Synonym(s):

Anti-γ-Aminobutyric Acid Type A Receptor (γ2 subunit)

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
Conjugate:
unconjugated
Clone:
polyclonal
Application:
western blot
Species reactivity:
bovine, mouse, rat, human
Citations:
2
Technique(s):
western blot: 1:200 using rat brain membrane
Uniprot accession no.:
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Product Name

Anti-GABAA Receptor (γ2 subunit) (extracellular) antibody produced in rabbit, affinity isolated antibody, lyophilized powder

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

lyophilized powder

species reactivity

bovine, mouse, rat, human

technique(s)

western blot: 1:200 using rat brain membrane

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... GABRG2(2566)
mouse ... Gabrg2(14406)
rat ... Gabrg2(29709)

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.

Immunogen

synthetic peptide corresponding to amino acids 39-53 of rat GABAA receptor (γ2 subunit). The sequence is identical in human, mouse, and bovine. In chick, it is 13/15 residues identical.

Physical form

Lyophilized from phosphate buffered saline, pH 7.4, 1% BSA, and 0.05% sodium azide.

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

常规特殊物品
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Carolina A Oliva et al.
International journal of molecular sciences, 24(2) (2023-01-22)
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Ann J Johnston et al.
Neurobiology of disease, 64, 131-141 (2014-01-11)
Genetic mutations in voltage-gated and ligand-gated ion channel genes have been identified in a small number of Mendelian families with genetic generalised epilepsies (GGEs). They are commonly associated with febrile seizures (FS), childhood absence epilepsy (CAE) and particularly with generalised

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