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Read our guarantee »Products:Tags & Cell Markers >> Epitope Tags >> Myc Tag
Anti-Myc tag antibody - ChIP Grade
See all Myc tag products (16) ...
Goat polyclonal to Myc tag - ChIP Grade
Antibody was verified by ELISA against peptide conjugated to BSA (EQKLISEEDL /BSA).
IP, ChIP, IHC-Fr, ICC/IF, WB, ICC, ELISAmore details
Liquid
Store at +4°C.
PBS with 0.1% sodium azide
Concentration information loading...
Immunogen affinity purified
Antibodies were affinity purified using the peptide immobilized on solid support. Antibody concentration was determined by extinction coefficient: absorbance at280 nm of 1.4 equals 1.0 mg of IgG.
Polyclonal
IgG
Epigenetics and Nuclear Signaling >> ChIP'ing antibodies >> ChIP'ing antibodies
Tags & Cell Markers >> Epitope Tags >> Myc Tag
Our Abpromise guarantee covers the use of ab9132 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IP: Use at an assay dependent dilution. (PubMed: 20224777)
ChIP: Use at an assay dependent dilution. (ChIP was performed with 25 ug chromatin, 5ug of antibody and 20 ul of Protein A/G beads.)
IHC-Fr: 1/50
ICC/IF: Use at an assay dependent concentration.
WB: 1/1000 - 1/30000.
ICC: 1/200 - 1/2000.
ELISA: 1/100 - 1/500.
Epitope tags are short peptide sequences that are easily recognized by tag-specific antibodies. Due to their small size, epitope tags do not affect the tagged protein’s biochemical properties. Most often sequences encoding the epitope tag are included with target DNA at the time of cloning to produce fusion proteins containing the epitope tag sequence. This allows anti-epitope tag antibodies to serve as universal detection reagents for any tag containing protein produced by recombinant means. This means that anti-epitope tag antibodies are a useful alternative to generating specific antibodies to identify, immunoprecipitate or immunoaffinity purify a recombinant protein. The anti-epitope tag antibody is usually functional in a variety of antibody-dependent experimental procedures. Expression vectors producing epitope tag fusion proteins are available for a variety of host expression systems including bacteria, yeast, insect and mammalian cells.
ChIP - Myc tag antibody - ChIP Grade (ab9132)

A stably transfected 293T human cell line harbouring the GAL4 upstream activation sequence was transiently transfected with a Myc or His - tagged GAL4 DNA Binding Domain construct. 48 hours post transfection Chromatin was prepared according to the Abcam X-ChIP protocol. The ChIP was performed with 25 ug chromatin, 5ug of antibody and 20 ul of Protein A/G beads. A non-specific antibody was used as the negative control. The immunoprecipitated DNA was quantified by real time PCR (SYBR Green approach).
Immunocytochemistry/ Immunofluorescence - Myc tag antibody - ChIP Grade (ab9132)

ab9132, at 1/500, tagging the Myc epitope in human Hela cells by immunocytochemistry/ immunofluorescence. Cells were paraformaldehyde fixed and permeabilized in 0.15% Triton prior to blocking in 10% serum for 1 hour at 23°C. The primary antibody incubated with the sample for 1 hour at 23°C. A donkey polyclonal anti-mouse antibody, diluted 1/500, was used as the secondary.
This image is courtesy of an anonymous Abreview.
This product has been referenced in:
See all 7 publications for this product
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A stably transfected 293T human cell line harbouring the GAL4 upstream activation sequence was transiently transfected with a Myc or His - tagged GAL4 DNA Binding Domain construct. 48 hours post transfection Chromatin was prepared according to the Abcam X-ChIP protocol. The ChIP was performed with 25 ug chromatin, 5ug of antibody and 20 ul of Protein A/G beads. A non-specific antibody was used as the negative control. The immunoprecipitated DNA was quantified by real time PCR (SYBR Green approach).

ab9132, at 1/500, tagging the Myc epitope in human Hela cells by immunocytochemistry/ immunofluorescence. Cells were paraformaldehyde fixed and permeabilized in 0.15% Triton prior to blocking in 10% serum for 1 hour at 23°C. The primary antibody incubated with the sample for 1 hour at 23°C. A donkey polyclonal anti-mouse antibody, diluted 1/500, was used as the secondary.
This image is courtesy of an anonymous Abreview.
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