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Merck
CN

G1166

Anti-GAD65 Antibody

mouse monoclonal, GAD-6

别名:

Anti-GAD 65

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
Conjugate:
unconjugated
Clone:
GAD-6, monoclonal
Application:
immunohistochemistry
western blot
Species reactivity:
mammals (and some lower vertebrates)
Citations:
11
Technique(s):
immunohistochemistry: 1:100-1:500
western blot: 1:1,000-1:5,000
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产品名称

Monoclonal Anti-Glutamic Acid Decarboxylase 65 antibody produced in mouse, clone GAD-6, purified immunoglobulin, buffered aqueous solution

biological source

mouse

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

GAD-6, monoclonal

form

buffered aqueous solution

species reactivity

mammals (and some lower vertebrates)

technique(s)

immunohistochemistry: 1:100-1:500
western blot: 1:1,000-1:5,000

isotype

IgG2a

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... GAD2(2572)
mouse ... Gad2(14417)

Biochem/physiol Actions

Recognizes the lower molecular weight isoform of the two GAD isoforms identified in brain, GAD 65. Can be used for immunochemical localization of GABA secreting neurons.

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

purified rat brain GAD 65.

Physical form

Solution in 0.01 M phosphate buffered saline, containing 0.04% sodium azide.

Preparation Note

Purified using Protein A chromatography.

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存储类别

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Stathis S Leondopulos et al.
Journal of neural engineering, 9(2), 026015-026015 (2012-03-01)
Slow wave oscillations in the brain are essential for coordinated network activity but have not been shown to self-organize in vitro. Here, the development of dissociated hippocampal neurons into an active network with oscillations on multi-electrode arrays was evaluated in
Han-Byeol Kim et al.
Cell death discovery, 6, 73-73 (2020-08-21)
Neonatal maternal separation (NMS), as an early-life stress (ELS), is a risk factor to develop emotional disorders. However, the exact mechanisms remain to be defined. In the present study, we investigated the mechanisms involved in developing emotional disorders caused by
Azadeh Yazdan-Shahmorad et al.
eLife, 7 (2018-05-29)
Brain stimulation modulates the excitability of neural circuits and drives neuroplasticity. While the local effects of stimulation have been an active area of investigation, the effects on large-scale networks remain largely unexplored. We studied stimulation-induced changes in network dynamics in
Rossella De Cegli et al.
Nucleic acids research, 41(2), 711-726 (2012-11-28)
Gene expression profiles can be used to infer previously unknown transcriptional regulatory interaction among thousands of genes, via systems biology 'reverse engineering' approaches. We 'reverse engineered' an embryonic stem (ES)-specific transcriptional network from 171 gene expression profiles, measured in ES
Susanna Molas et al.
Nature neuroscience, 20(9), 1260-1268 (2017-07-18)
Novelty preference (NP) is an evolutionarily conserved, essential survival mechanism often dysregulated in neuropsychiatric disorders. NP is mediated by a motivational dopamine signal that increases in response to novel stimuli, thereby driving exploration. However, the mechanism by which once-novel stimuli

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