04-1643
Rabbit Anti-Mouse IgG Antibody, clone RM104
clone RM104, from rabbit
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438,00 €
A propos de cet article
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Source biologique
rabbit
Niveau de qualité
Forme d'anticorps
purified antibody
Type de produit anticorps
secondary antibodies
Clone
RM104, monoclonal
Espèces réactives
mouse
Technique(s)
ELISA: suitable
western blot: suitable
Isotype
IgG
Conditions d'expédition
wet ice
Modification post-traductionnelle de la cible
unmodified
1 of 4
Cet article | 06-371 | 04-1648 | SAB5600195 |
|---|---|---|---|
| clone RM104, monoclonal | clone polyclonal | clone RMG01, monoclonal | clone RM104, monoclonal, recombinant monoclonal |
| biological source rabbit | biological source rabbit | biological source goat | biological source - |
| species reactivity mouse | species reactivity mouse | species reactivity rabbit | species reactivity mouse |
| antibody form purified antibody | antibody form purified immunoglobulin | antibody form purified antibody | antibody form purified immunoglobulin |
| technique(s) ELISA: suitable, western blot: suitable | technique(s) immunoprecipitation (IP): suitable | technique(s) ELISA: suitable, western blot: suitable | technique(s) ELISA: 0.005-0.2 μg/mL, immunocytochemistry: 0.5-2 μg/mL, immunohistochemistry: 0.5-2 μg/mL, immunoprecipitation (IP): suitable (assay dependent concentration), western blot: 0.1— 0.5 μg/mL |
| shipped in wet ice | shipped in dry ice | shipped in wet ice | shipped in wet ice |
Immunogène
Application
Secondary & Control Antibodies
Secondary Antibodies Adsorbed for Dual Labeling
Actions biochimiques/physiologiques
Forme physique
Notes préparatoires
Note: Variability in freezer temperatures below -20°C may cause glycerol containing solutions to become frozen during storage.
Remarque sur l'analyse
Autres remarques
Clause de non-responsabilité
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Code de la classe de stockage
12 - Non Combustible Liquids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
does not flash
Point d'éclair (°C)
does not flash
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Contenu apparenté
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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