제품 이름
Anti-EEA1 antibody, Mouse monoclonal, clone EEA1-N19, purified from hybridoma cell culture
biological source
mouse
conjugate
unconjugated
antibody form
purified from hybridoma cell culture
antibody product type
primary antibodies
clone
EEA1-N19, monoclonal
form
buffered aqueous solution
mol wt
antigen ~160 kDa
species reactivity
human, mouse, rat
concentration
~1.0 mg/mL
technique(s)
immunoprecipitation (IP): suitable
indirect immunofluorescence: suitable
western blot: 1-2 μg/mL using whole extract of rat NRK cells
isotype
IgG2a
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Quality Level
Gene Information
human ... EEA1(8411)
mouse ... Eea1(216238)
rat ... Eea1(314764)
Application
Anti-EEA1 antibody, Mouse monoclonalhas been used in:
- immunoblotting
- immunoprecipitation
- cell fractionation
- indirect immunofluorescence
- immunohistochemistry
Monoclonal Anti-EEA1 antibody produced in mouse is suitable for the following applications:
- Immunoprecipitation
- Indirect immunofluorescence
- Western blotting at a concentration of 1-2μg/mL using whole extract of rat NRK cells
Biochem/physiol Actions
Early Endosome Antigen 1 (EEA1) FYVE domain is involved in intracellular trafficking and is implicated in the specific localization of EEA1 to endosomes . Endosomal targeting of EEA1 also requires its binding to the active form of the small GTPase Rabaptin-5 (Rab5). The binding of EEA1 to phosphatidylinositol 3-phosphate (PtdIns 3P) and Rab5-GTP is essential for the localization and function of EEA1 in endocytic membrane fusion. Monoclonal Anti-EEA1 may be used as an early endosome marker.
Early Endosome Antigen 1 (EEA1) controls vesicle fusion during endocytosis. In neurons, it is involved in recycling of synaptic vesicles and neurotransmitter receptors. Patients with neurological deficits develop EEA1 autoantibodies. Mutation in EEA1 gene leads to susceptibility to diabetes in the Japanese population. Phosphatidylinositol 3-phosphate (PtdIns(3)P) is essential for the localization and function of EEA1.
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.
General description
Monoclonal Anti-EEA1 (mouse IgG2a isotype) is derived from the hybridoma EEA1-N19 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide corresponding to a fragment of human EEA1. Early Endosome Antigen 1 (EEA1) is a dimer. It comprises extensive coiled-coil regions, and at its C-terminus contains a cysteine-rich zinc-finger-like domain named FYVE domain.
The gene Early Endosome Antigen 1 (EEA1) encodes for around 1400 amino acid proteins. It is a peripheral membrane protein associated with the cytoplasmic face of early endosomes. EEA1 is a autoantigen associated with subacute cutaneous systemic lupus erythematosus and is a coiled-coil protein localized to early endosomes and cytosol.
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
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저장 등급
12 - Non Combustible Liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
Timely regulated sorting from early to late endosomes is required to maintain cerebellar long-term depression
Kim T, et al.
Nature Communications, 8(1), 401-401 (2017)
Cellular functions of phosphatidylinositol 3-phosphate and FYVE domain proteins
GILLOOLY DJ, et al.
The Biochemical Journal, 355, 249-258 (2001)
Taegon Kim et al.
Nature communications, 8(1), 401-401 (2017-09-03)
An important feature of long-term synaptic plasticity is the prolonged maintenance of plastic changes in synaptic transmission. The trafficking of AMPA-type glutamate receptors (AMPARs) is involved in the expression of many forms of synaptic plasticity, yet the subsequent events accomplishing
Early Endosome Antigen 1 (EEA1) decreases in macrophages infected with Paracoccidioides brasiliensis
Voltan AR, et al.
Medical Mycology, 51(7), 759-764 (2013)
Anna A Cook et al.
eLife, 12 (2023-12-12)
Spinocerebellar ataxia type 6 (SCA6) is a rare disease that is characterized by cerebellar dysfunction. Patients have progressive motor coordination impairment, and postmortem brain tissue reveals degeneration of cerebellar Purkinje cells and a reduced level of cerebellar brain-derived neurotrophic factor
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