G6160
Monoclonal Anti-β-COP antibody produced in mouse
clone maD, ascites fluid
Synonym(s):
Anti-BARMACS, Anti-COPB
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About This Item
Conjugate:
unconjugated
Clone:
maD, monoclonal
Application:
ARR, IF, WB
Citations:
25
biological source
mouse
conjugate
unconjugated
antibody form
ascites fluid
antibody product type
primary antibodies
clone
maD, monoclonal
contains
15 mM sodium azide
species reactivity
human, rat, hamster, monkey
technique(s)
indirect immunofluorescence: 1:80 using cultured Chinese hamster ovary (CHO) cells, microarray: suitable, western blot: 1:1,000 using a preparation of stacked Golgi membranes from rat liver
isotype
IgG1
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... COPB1(1315)
rat ... Copb1(114023)
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General description
The coatomer (approx. 550kDa) consists of proteins designated α-, β-, γ-, and δ-COP, together with substoichiometric amounts of several other proteins.
Immunogen
synthetic peptide D1 of β-COP (a.a. 701-715) conjugated to KLH
Application
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunofluorescence (1 paper)
Immunofluorescence (1 paper)
Monoclonal Anti-β-COP antibody produced in mouse is suitable for use as a primary antibody in immunoblot:
It is suitable for immunostaining of β-coatomer, that is used as a intracellular, Golgi protein marker :
It is suitable for use in cell-surface ELISA of human aortic endothelial cells (HAEC)
It is also suitable for western blot analysis at a working dilution of 1:1000 using a preparation of stacked Golgi membranes from rat liver, for indirect immunofluorescence at a working dilution of 1:80 using cultured Chinese hamster ovary (CHO) cells and for microarray.
- analysis at a working dilution of 1:1000 using subcellular proteins from rat PC12 (pheochromocytoma) cells
- analysis of gradient fractions of cerebral microvessels to confirm the separation of plasma membrane lipid raft domains from intracellular membranous components
- detection of the Golgi marker protein β-COP in exosome-enriched extracellular microvesicles (eMV) preparations from untreated HeLa cells
It is suitable for immunostaining of β-coatomer, that is used as a intracellular, Golgi protein marker :
- to confirm that CD14 staining is localized to the cell surface of HAEC
- for examining the localization of Meltrin β in the Golgi apparatus and its vicinity in neurons prepared from developing dorsal root ganglia of mouse embryos
- in NB4 and NB4-LR1 cells to examine the colocalization of PKA regulatory subunits
- in CHO cells to examine colocalization of GFP-Rab24
It is suitable for use in cell-surface ELISA of human aortic endothelial cells (HAEC)
It is also suitable for western blot analysis at a working dilution of 1:1000 using a preparation of stacked Golgi membranes from rat liver, for indirect immunofluorescence at a working dilution of 1:80 using cultured Chinese hamster ovary (CHO) cells and for microarray.
Biochem/physiol Actions
COPs (coatomer proteins) contain adaptin-like, complex (8) and are transiently attached to the vesicles involved in transport within the Golgi complex and possibly between the rough ER and Golgi complex. β-COP has a molar mass of 110kDa and its primary structure is homologous to the β-adaptin component of clathrin-coated vesicles.
The antibody recognizes an epitope in the β-COP protein (110 kDa) and stains the periphery of the Golgi complex using immunocytochemical techniques.
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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Storage Class
10 - Combustible liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
动植物来源生物产品
常规特殊物品
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Daniela B Munafó et al.
Traffic (Copenhagen, Denmark), 3(7), 472-482 (2002-06-06)
Rab GTPases comprises a large family of proteins, with more than 50 gene products localized in distinct subcellular compartments. Rab24 is a member of this family whose function is not presently known. In order to elucidate the role of this
Neuronal adaptor FE65 stimulates Rac1-mediated neurite outgrowth by recruiting and activating ELMO1.
Wen Li et al.
The Journal of biological chemistry, 293(20), 7674-7688 (2018-04-05)
Neurite outgrowth is a crucial process in developing neurons for neural network formation. Understanding the regulatory mechanisms of neurite outgrowth is essential for developing strategies to stimulate neurite regeneration after nerve injury and in neurodegenerative disorders. FE65 is a brain-enriched
Jeffrey Hewett et al.
Journal of neuroscience research, 72(2), 158-168 (2003-04-03)
Most cases of early-onset torsion dystonia are caused by deletion of GAG in the coding region of the DYT1 gene encoding torsinA. This autosomal dominant neurologic disorder is characterized by abnormal movements, believed to originate from neuronal dysfunction in the
Kimberly A Walton et al.
The Journal of biological chemistry, 278(32), 29661-29666 (2003-06-05)
We demonstrated previously that oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (ox-PAPC) and, specifically, the component lipid 1-palmitoyl-2-(5,6-epoxyisoprostane E2)-sn-glycero-3-phosphorylcholine increase interleukin-8 (IL-8) synthesis in aortic endothelial cells. The goal of the current studies was to characterize the receptor complex mediating the increased transcription of IL-8.
J A Whitney et al.
Cell, 83(5), 703-713 (1995-12-01)
Endosomes are intermediates for a complex series of sorting and transport events that occur during receptor-mediated endocytosis. These involve the recognition of targeting determinants on the cytoplasmic domains of many membrane proteins as well as the formations of specific transport
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