SAB5300161
Monoclonal Anti-Ractopamine antibody produced in mouse
clone Rac1, ascites fluid
别名:
N/A
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关于此项目
NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
Rac1, monoclonal
Application:
ELISA (d), WB
Citations:
5
biological source
mouse
Quality Level
conjugate
unconjugated
antibody form
ascites fluid
antibody product type
primary antibodies
clone
Rac1, monoclonal
species reactivity
human
technique(s)
direct ELISA: 1:10,000, western blot: 1:500-1:2,000
isotype
IgG
shipped in
wet ice
storage temp.
−20°C
target post-translational modification
unmodified
Immunogen
Rac-OVA.
Mouse monoclonal antibody raised against Ractopamine
Mouse monoclonal antibody raised against Ractopamine
Physical form
Ascitic fluid containing 0.03% sodium azide.
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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存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Cansu Karabiyik et al.
Brain pathology (Zurich, Switzerland), 28(4), 569-580 (2017-09-30)
The Rho GTPase Rac1 is a multifunctional protein involved in distinct pathways ranging from development to pathology. The aim of the present study was to unravel the contribution of neuronal Rac1 in regulating the response to brain injury induced by
Wenjing Ruan et al.
Molecular biology of the cell, 19(8), 3192-3202 (2008-05-30)
Members of the tumor necrosis factor receptor (TNFR) superfamily control cell fate determination, including cell death and differentiation. Fas (CD95) is the prototypical "death receptor" of the TNFR superfamily and signals apoptosis through well established pathways. In the adult nervous
Diane Chan et al.
The Journal of biological chemistry, 286(18), 16140-16149 (2011-04-02)
Mutations in leucine-rich repeat kinase 2 (LRRK2) are currently the most common genetic cause of familial late-onset Parkinson disease, which is clinically indistinguishable from idiopathic disease. The most common pathological mutation in LRRK2, G2019S LRRK2, is known to cause neurite
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| SAB5300161-100UL | 04061837598449 |