04-1643

Rabbit Anti-Mouse IgG Antibody, clone RM104

Name: Rabbit Anti-Mouse IgG Antibody, clone RM104
Brand: MM

clone RM104, from rabbit

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About This Item

UNSPSC Code:

12352203

eCl@ss:

32160702

NACRES:

NA.46

Key Documents

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biological source

rabbit

Quality Level

100

antibody form

purified antibody

antibody product type

secondary antibodies

clone

RM104, monoclonal

species reactivity

mouse

technique(s)

ELISA: suitable
western blot: suitable

isotype

IgG

shipped in

wet ice

target post-translational modification

unmodified

Related Categories

Secondary Antibodies

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This Item	06-371	04-1648	SAB5600195
Sigma-Aldrich 04-1643 Rabbit Anti-Mouse IgG Antibody, clone RM104	Sigma-Aldrich 06-371 Rabbit Anti-Mouse IgG Antibody	Sigma-Aldrich 04-1648 Goat Anti-Rabbit IgG Fab Antibody, clone RMG01	Sigma-Aldrich SAB5600195 Anti-Mouse IgG antibody, Rabbit monoclonal
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

Immunogen

Mouse IgG

Application

Research Category
Secondary & Control Antibodies

Research Sub Category
Secondary Antibodies Adsorbed for Dual Labeling

This rabbit monoclonal Rabbit Anti-Mouse IgG, clone RM104, Cat. No. 04-1643 is validated for use in ELISA and Western Blotting, for the detection of Mouse IgG.

Western Blotting Analysis (WB): 0.2 μg/mL from a representative lot detected Mouse IgG in nonreduced (-) mouse immunoglobulins.

Biochem/physiol Actions

This antibody reacts to the Fc region of all subclasses of mouse IgG. No cross reactivity with mouse IgM, IgA, IgE, human IgG, and rat IgG. It may cross react to goat IgG. The Fc region of RM104 has been engineered to eliminate the binding of Fc receptor.

Physical form

Format: Purified

Protein A purified

Rabbit monoclonal in PBS with 1% BSA and 0.09% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of receipt.
Note: Variability in freezer temperatures below -20°C may cause glycerol containing solutions to become frozen during storage.

Analysis Note

ELISA Analysis: The specificity and reactivity of a representative lot was confirmed by ELISA analyses.

Other Notes

Concentration: Please refer to lot specific datasheet.

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 Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

does not flash

Flash Point(C)

does not flash

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Characterization of Estrogen Receptor α Phosphorylation Sites in Breast Cancer Tissue Using the SNAP i.d® 2.0 System

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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