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Read our guarantee »Anti-MyoD1 antibody [5.2F]
See all MyoD1 products (10) ...
Mouse monoclonal [5.2F] to MyoD1
This antibody does not cross react with Myogenin, Myf5, or Myf6.
ICC/IF, Sandwich ELISA, ELISA, IF, IP, IHC-P, IHC-Fr, Electron Microscopy, WBmore details
Reacts with
Mouse, Rat, Chicken, Human
Predicted to work with
Sheep, Cow, Pig
Synthetic peptide: LLSPPLRDIDLTGPDGSLCSFETADDFYDDPCFDSPDLRF FEDLDPRLVHVGAL, corresponding to N terminal amino acids 3-56 of Mouse Myogenin D1.
LLSPPLRDID LTGPDGSLCS FETADDFYDD PCFDSPDLRF FEDLDPRLVH VGAL
Rhabdomyosarcoma.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.08% Sodium Azide
Constituents: PBS
Concentration information loading...
IgG fraction
Monoclonal
5.2F
Sp2/0-Ag14
IgG2a
Developmental Biology >> Organogenesis >> Skeletal development >> Muscle
Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> HLH / Leucine Zipper >> HLH
Our Abpromise guarantee covers the use of ab16148 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use at an assay dependent dilution.
sELISA: Use a concentration of 5 µg/ml Can be paired for Sandwich ELISA with Rabbit polyclonal to MyoD1 (ab64159). (For sandwich ELISA, use this antibody as Capture at 5 µg/ml with Rabbit polyclonal to MyoD1 (ab64159) as Detection.)
ELISA: Use at an assay dependent dilution.
IF: Use at an assay dependent dilution.
IP: Use at 2 µg/mg of lysate.
IHC-P: Use a concentration of 2 - 4 µg/ml.
IHC-Fr: Use a concentration of 2 - 4 µg/ml.
EM: Use at an assay dependent dilution.
WB: Use a concentration of 1 µg/mlPredicted molecular weight: 35 kDa.
Involved in muscle differentiation (myogenic factor). Induces fibroblasts to differentiate into myoblasts. Activates muscle-specific promoters. Interacts with and is inhibited by the twist protein. This interaction probably involves the basic domains of both proteins.
Contains 1 basic helix-loop-helix (bHLH) domain.
Acetylated by a complex containing EP300 and PCAF. The acetylation is essential to activate target genes. Conversely, its deacetylation by SIRT1 inhibits its function.
Ubiquitinated on the N-terminus; which is required for proteasomal degradation.
Nucleus.
Target information above from: UniProt accessionP15172
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Sandwich ELISA - MyoD1 antibody [5.2F] (ab16148)
![Sandwich ELISA - MyoD1 antibody [5.2F] (ab16148)](/ps/datasheet/images/16/ab16148/MyoD1-Primary-antibodies-ab16148-5.jpg)
Standard Curve for Myo-D; dilution range 1 pg/ml to 1 ug/ml using Capture Antibody Mouse monoclonal [5.2F] to MyoD1 (ab16148) at 5ug/ml and Detector Antibody Rabbit polyclonal to MyoD1 (ab64159) at 0.1ug/ml.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - MyoD1 antibody [5.2F] (ab16148)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - MyoD1 antibody [5.2F] (ab16148)](/ps/datasheet/Images/16/ab16148/ab16148.jpg)
Immunohistochemical staining using ab16148 at 2ug/ml on formalin fixed, paraffin embedded samples of human rhabdomyosarcoma.
Immunocytochemistry/ Immunofluorescence - MyoD1 antibody [5.2F] (ab16148)
![Immunocytochemistry/ Immunofluorescence - MyoD1 antibody [5.2F] (ab16148)](/ps/datasheet/images/16/ab16148/MyoD1-Primary-antibodies-ab16148-4.jpg)
ab16148 staining MyoD1 in rat differentiated skeletal muscle cells by Immunocytochemistry/ Immunofluorescence. The cells were fixed in paraformaldehyde and then blocked using 2% serum for 1 hour. Samples were then incubated with primary antibody at 1/200 for 8 hours. The secondary antibody used was a goat anti-mouse IgG conjugated to Alexa Fluor® 488 (green) used at a 1/1000 dilution. DAPI was used to stain the cell nuclei (blue).
Image courtesy of an Abreview submitted by Mal Niladri.
This product has been referenced in:
See all 6 publications for this product
Publishing research using ab16148? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
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![Sandwich ELISA - MyoD1 antibody [5.2F] (ab16148)](/ps/datasheet/images/16/ab16148/MyoD1-Primary-antibodies-ab16148-5.jpg)
Standard Curve for Myo-D; dilution range 1 pg/ml to 1 ug/ml using Capture Antibody
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - MyoD1 antibody [5.2F] (ab16148)](/ps/datasheet/Images/16/ab16148/ab16148.jpg)
Immunohistochemical staining using ab16148 at 2ug/ml on formalin fixed, paraffin embedded samples of human rhabdomyosarcoma.
![Immunocytochemistry/ Immunofluorescence - MyoD1 antibody [5.2F] (ab16148)](/ps/datasheet/images/16/ab16148/MyoD1-Primary-antibodies-ab16148-4.jpg)
ab16148 staining MyoD1 in rat differentiated skeletal muscle cells by Immunocytochemistry/ Immunofluorescence. The cells were fixed in paraformaldehyde and then blocked using 2% serum for 1 hour. Samples were then incubated with primary antibody at 1/200 for 8 hours. The secondary antibody used was a goat anti-mouse IgG conjugated to Alexa Fluor® 488 (green) used at a 1/1000 dilution. DAPI was used to stain the cell nuclei (blue).
Image courtesy of an Abreview submitted by Mal Niladri.
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