ST1684
Anti-MAG Mouse mAb (3C7)
liquid, clone 3C7, Calbiochem®
别名:
Anti-Myelin Associated Glycoprotein
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关于此项目
NACRES:
NA.41
UNSPSC Code:
12352203
Clone:
3C7, monoclonal
Species reactivity:
human
Application:
—
Citations:
1
biological source
mouse
antibody form
purified antibody
antibody product type
primary antibodies
clone
3C7, monoclonal
form
liquid
does not contain
preservative
species reactivity
human
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, avoid repeated freeze/thaw cycles
dilution
(Immunoblotting (1-5 µg/mL) Paraffin Sections (3 µg/mL))
isotype
IgG1
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... MAG(4099)
General description
Purified mouse monoclonal antibody. Recognizes the ~50-52 kDa MAG protein.
Recognizes the ~50-52 kDa MAG protein in Jurkat cells and human cerebellum tissue.
This Anti-MAG Mouse mAb (3C7) is validated for use in Immunoblotting Paraffin Sections for the detection of MAG.
Immunogen
A recombinant polypeptide corresponding to amino acids of 119-209 human MAG, expressed as a GST fusion protein
Application
Immunoblotting (1-5 µg/ml)Paraffin Sections (3 µg/ml)
Physical form
In PBS, pH 7.2.
Preparation Note
Following initial thaw, aliquot and freeze (-20°C).
Analysis Note
Positive Control
Jurkat cells, human cerebellum tissue
Jurkat cells, human cerebellum tissue
Other Notes
Variables associated with assay conditions will dictate the proper working dilution.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Regulatory Review (Z)
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存储类别
12 - Non Combustible Liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Xiaolin Hou et al.
Molecular medicine reports, 17(3), 4515-4523 (2018-01-19)
Oligodendrocytes (OLs) are myelin-forming cells that are present within the central nervous system. Impaired oligodendrocyte precursor cell (OPC) differentiation into mature OLs is a major cause of demyelination diseases. Therefore, identifying the underlying molecular mechanisms of OPC differentiation is crucial
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