推荐产品
生物源
rat
品質等級
抗體表格
culture supernatant
抗體產品種類
primary antibodies
無性繁殖
14, monoclonal
物種活性（以同源性預測）
mammals
製造商／商標名
Chemicon®
技術
ELISA: suitable
immunohistochemistry: suitable
同型
IgG2b
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
目標翻譯後修改
unmodified
基因資訊
human ... MBP(4155)
特異性
Reacts with a synthetic peptide corresponding to human MBP sequence 36-50 as well as intact human MBP. Numbering of MBP residues is as described by Martenson (1984). Mapped by Geyson method to FFGGDR and RFFGGO region.
免疫原
Bovine myelin basic protein.
Epitope: a.a. 36-50
應用
Detect Myelin Basic Protein using this Anti-Myelin Basic Protein Antibody, a.a. 36-50, clone 14 validated for use in ELISA, IH.
Immunohistochemistry (frozen sections)
ELISA
This antibody is also expected to work for Western blot. Specific testing has not been performed.
Optimal working dilutions must be determined by end user.
ELISA
This antibody is also expected to work for Western blot. Specific testing has not been performed.
Optimal working dilutions must be determined by end user.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Neuronal & Glial Markers
Neurochemistry & Neurotrophins
Neuronal & Glial Markers
Neurochemistry & Neurotrophins
聯結
Replaces: MAB395
外觀
Tissue culture supernatant. Liquid containing 0.09% sodium azide.
儲存和穩定性
Maintain at -20° in undiluted aliquots for up to 12 months after date of receipt. Avoid repeated freeze-thaw cycles.
法律資訊
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
免責聲明
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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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
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The Journal of biological chemistry, 289(3), 1629-1638 (2013-11-28)
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Functional screening for compounds that promote remyelination represents a major hurdle in the development of rational therapeutics for multiple sclerosis. Screening for remyelination is problematic, as myelination requires the presence of axons. Standard methods do not resolve cell-autonomous effects and
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