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Read our guarantee »Products:Cell Biology >> Cell Cycle >> Kinases/Phosphatases >> Cdk Regulators
Anti-DBF4 antibody
DBF4 抗体 (5件) 一覧
Rabbit polyclonal to DBF4
ab70134 detects endogenous levels of total DBF4 protein.
ICC/IF, WB, ELISAmore details
Reacts with
Mouse, Human
Synthetic peptide derived from the N terminus of human DBF4.
NIH3T3 cell extracts treated with H2O2 (100µM, 30mins), COS7 cell extracts treated with PMA (125mg/ml, 30mins), and NIH3T3 cell extracts treated with both H2O2 (100µM, 30mins) and PMA (125mg/ml, 30mins).
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS (without Mg2+ and Ca2+), 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
ab70124 was affinity purified from rabbit antiserum by affinity chromatography using epitope specific immunogen.
Polyclonal
IgG
Epigenetics and Nuclear Signaling >> DNA / RNA >> DNA Synthesis >> Other
Cell Biology >> Cell Cycle >> Kinases/Phosphatases >> Cdk Regulators
Our Abpromise guarantee covers the use of ab70134 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 a concentration of 1 µg/ml
WB: 1/500 - 1/1000.Detects a band of approximately 77 kDa (predicted molecular weight: 77 kDa).
ELISA: 1/10000
Regulatory subunit for CDC7 which activates its kinase activity thereby playing a central role in DNA replication and cell proliferation. Required for progression of S phase. The complex CDC7-DBF4A selectively phosphorylates MCM2 subunit at 'Ser-40' and 'Ser-53' and then is involved in regulating the initiation of DNA replication during cell cycle.
Highly expressed in testis and thymus. Expressed also in most cancer cells lines.
Contains 2 BRCT domains.
Contains 1 DBF4-type zinc finger.
Phosphorylated upon DNA damage, probably by ATM or ATR.
Nucleus.
Target information above from: UniProt accessionQ9UBU7
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - DBF4 antibody (ab70134)

All lanes : Anti-DBF4 antibody (ab70134) at 1/500 dilution
Lane 1 : NIH3T3 cell extracts
treated with H2O2 (100µM, 30mins) at 5 µg
Lane 2 : COS7 cell extracts
treated with PMA (125mg/ml, 30mins)
Lane 3 : NIH3T3 cell extracts
treated with H2O2 (100µM, 30mins) and PMA (125mg/ml, 30mins) with immunising peptide at 5 µg
Predicted band size : 77 kDa
Observed band size : 77 kDa
Additional bands at : 60 kDa. We are unsure as to the identity of these extra bands.
Immunocytochemistry/ Immunofluorescence-DBF4 antibody(ab70134)

ICC/IF image of ab70134 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab70134, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
ab70134 has not yet been referenced specifically in any publications.
Publishing research using ab70134? Please let us know so that we can cite the reference in this datasheet
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All lanes : Anti-DBF4 antibody (ab70134) at 1/500 dilution
Lane 1 : NIH3T3 cell extracts
treated with H2O2 (100µM, 30mins) at 5 µg
Lane 2 : COS7 cell extracts
treated with PMA (125mg/ml, 30mins)
Lane 3 : NIH3T3 cell extracts
treated with H2O2 (100µM, 30mins) and PMA (125mg/ml, 30mins) with immunising peptide at 5 µg
Predicted band size : 77 kDa
Observed band size : 77 kDa
Additional bands at : 60 kDa. We are unsure as to the identity of these extra bands.

ICC/IF image of ab70134 stained HeLa cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab70134, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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