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Fortfahren mit
biological source
rabbit
conjugate
unconjugated
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
purified by
affinity chromatography
species reactivity
rat, human, mouse
species reactivity (predicted by homology)
porcine (based on 100% sequence homology), feline (based on 100% sequence homology), horse (based on 100% sequence homology), hamster (based on 100% sequence homology), bovine (based on 100% sequence homology)
technique(s)
immunoprecipitation (IP): suitable, western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Quality Level
Gene Information
human ... MAPKAP1(79109)
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Dieser Artikel | |||
|---|---|---|---|
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level 100 |
| biological source rabbit | biological source mouse | biological source rabbit | biological source rabbit |
| antibody form affinity isolated antibody | antibody form purified antibody | antibody form affinity isolated antibody | antibody form affinity isolated antibody |
| species reactivity rat, human, mouse | species reactivity rat, mouse, human | species reactivity human | species reactivity human |
| Gene Information human ... MAPKAP1(79109) | Gene Information human ... MAPKAP1(79109) | Gene Information human ... RAC1(5879) | Gene Information human ... MAPKAP1(79109) |
| technique(s) immunoprecipitation (IP): suitable, western blot: suitable | technique(s) immunofluorescence: suitable, immunohistochemistry: suitable (paraffin), immunoprecipitation (IP): suitable, western blot: suitable | technique(s) immunoprecipitation (IP): suitable, western blot: suitable | technique(s) inhibition assay: suitable (peptide), western blot: suitable |
General description
Immunogen
Application
Signaling
Signaling Neuroscience
Biochem/physiol Actions
Physical form
Preparation Note
Analysis Note
Western Blotting Analysis: A 1:500 dilution of this antibody detected mSin1 in 10 µg of A431 cell lysate.
Other Notes
Disclaimer
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Lagerklasse
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Analysenzertifikate (COA)
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Verwandter Inhalt
A major focus of breast cancer research is to understand the mechanisms responsible for disease progression and drug resistance. Toward that end, it has been found that approximately two thirds of all human breast carcinomas overexpress the Estrogen Receptor α (ERα) protein and it remains the primary pharmacological target for endocrine therapy1,2. The normal cellular function of ERα is as a transcription factor that mediates a wide variety of physiological processes, many of which are dependent upon phosphorylation of the receptor at specific amino acid residues3,4. Indeed, ERα is known to be phosphorylated at a multitude of different sites, yet how these all correlate to disease remains unclear5. Here, we interrogated multiple sites of ERα for phosphorylation status by screening an extensive panel of different breast cancer patient samples and other non-breast cancer tissue microarray (TMA) slide samples to determine their relevance to disease.
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