AB5354
Anti-Internexin α Antibody
serum, Chemicon®
別名:
Anti-NEF5, Anti-NF-66, Anti-NF66, Anti-TXBP-1
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この商品について
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
polyclonal
Application:
ELISA, ICC, IHC, WB
Citations:
12
biological source
rabbit
conjugate
unconjugated
antibody form
serum
antibody product type
primary antibodies
clone
polyclonal
species reactivity (predicted by homology)
mammals
manufacturer/tradename
Chemicon®
technique(s)
ELISA: suitable, immunocytochemistry: suitable, immunohistochemistry: suitable, western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Quality Level
Gene Information
human ... INA(9118)
Immunogen
Full length recombinant rat alpha-internexin fused to E. coli Trp E.
Application
Anti-Internexin Antibody, α is an antibody against Internexin for use in ELISA, WB, IC, IH.
Immunohistochemistry on formalin or paraformaldehyde fixed tissues.
Immunocytochemistry.
Western blot: using human or rat brain homogenates.
ELISA
Optimal working dilutions must be determined by end user.
Immunocytochemistry.
Western blot: using human or rat brain homogenates.
ELISA
Optimal working dilutions must be determined by end user.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Neurofilament & Neuron Metabolism
Neuronal & Glial Markers
Neurofilament & Neuron Metabolism
Neuronal & Glial Markers
Biochem/physiol Actions
alpha-internexin, C-terminal globular "tail" region. By western blot, AB5354 detects a major band at 66 kDa and a minor band at approximately 150 kDa corresponding to alpha internexin monomer and dimer, respectively. A minor band at approximately 50 kDa is occasionally detected and is believed to be a degradation product of alpha internexin. This antibody has been referred to in the literature as the R36 antibody (Evans, 2002).
Physical form
Serum liquid, containing no preservatives.
Preparation Note
Maintain frozen at -20°C in undiluted aliquots for up to 6 months after date of receipt. Avoid repeated freeze/thaw cycles.
Analysis Note
Control
POSITIVE CONTROL CELLS: PC12, Ntera2.
POSITIVE CONTROL CELLS: PC12, Ntera2.
Other Notes
Replaces: 04-1032
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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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保管分類
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
AB5354:
jan
試験成績書（COA）
製品のロット番号・バッチ番号を入力して、試験成績書（COA） を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Raymond S Roginski et al.
Gene, 648, 42-53 (2018-01-18)
The known functions of the human GCOM1 complex hub gene include transcription elongation and the intercalated disk of cardiac myocytes. However, in all likelihood, the gene's most interesting, and thus far least understood, roles will be found in the central
Frank Y Lee et al.
Journal of neuroscience research, 99(1), 67-89 (2020-05-22)
The function(s) of the Biogenesis of Lysosome-related Organelles Complex-1 (BLOC-1) during brain development is to date largely unknown. Here, we investigated how its absence alters the trajectory of postnatal brain development using as model the pallid mouse. Most of the
Motor unit abnormalities in Dystonia musculorum mice.
De Repentigny, Y; Ferrier, A; Ryan, SD; Sato, T; Kothary, R
Testing null
Peripherin is a subunit of peripheral nerve neurofilaments: implications for differential vulnerability of CNS and peripheral nervous system axons.
Yuan, A; Sasaki, T; Kumar, A; Peterhoff, CM; Rao, MV; Liem, RK; Julien, JP; Nixon, RA
The Journal of Neuroscience null
Tatsuo Suzuki et al.
Life science alliance, 4(7) (2021-05-20)
A purification protocol was developed to identify and analyze the component proteins of a postsynaptic density (PSD) lattice, a core structure of the PSD of excitatory synapses in the central nervous system. "Enriched"- and "lean"-type PSD lattices were purified by
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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