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Read our guarantee »Products:Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> Zinc Finger
Anti-GATA1 antibody
See all GATA1 products (13) ...
Rabbit polyclonal to GATA1
ab28839 recognises GATA-1.
WB, ELISA, IHC-P, IP, ICC/IFmore details
Reacts with
Mouse, Human
Synthetic non-phosphopeptide derived from human GATA1 around the phosphorylation site of Serine 142.
IHC: breast carcinoma WB: K562 cell line
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS (without Mg++ and Ca++), 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Our Abpromise guarantee covers the use of ab28839 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/500 - 1/1000.Detects a band of approximately 43 kDa (predicted molecular weight: 43 kDa).
ELISA: 1/10000
IHC-P: 1/50 - 1/100.
IP: Use at an assay dependent dilution.
ICC/IF: Use a concentration of 1 - 5 µg/ml.
GATA1 (Globin transcription factor 1) is a Cys2/Cys2 zinc finger DNA binding protein that is expressed primarily in erythroid, megakaryocytic, mast cells and eosinophilic cells. It belongs to the GATA family of transcription factors. GATA1 is a transcriptional activator which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence [AT]GATA[AG] within regulatory regions of globin genes and of other genes expressed in erythroid cells. The protein also plays an important role in erythroid development by regulating the switch from fetal hemoglobin production to adult hemoglobin. Mutations in this gene have been associated with X-linked dyserythropoietic anemia and thrombocytopenia. Acquired somatic mutations in GATA1 occur in virtually all children with Down's Syndrome, congenital transient myeloproliferative syndrome (TMD) and acute megakaryocytic leukemia.
Nuclear
Immunohistochemistry (Paraffin-embedded sections) - GATA1 antibody (ab28839)

Immunohistochemical analysis of paraffin-embedded breast carcinoma. Left: Using GATA-1(Ab-1) Antibody (ab28839); Right: The same antibody preincubated with synthesized peptide.
Western blot - GATA1 antibody (ab28839)

All lanes : Anti-GATA1 antibody (ab28839) (1/500-1/1000 dilution)
Lane 1 : extracts from K562 cells (5-30ug).
Lane 2 : extracts from K562 cells (5-30ug).
Predicted band size : 43 kDa
Observed band size : 43 kDa
Western blot analysis of extracts from K562 cells. Line1: Using GATA-1 antibody (ab28839); Line2: The same antibody preincubated with synthesized peptide.
Immunocytochemistry/ Immunofluorescence - GATA1 antibody (ab28839)

ICC/IF image of ab28839 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 (ab28839, 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.
This product has been referenced in:
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Immunohistochemical analysis of paraffin-embedded breast carcinoma. Left: Using GATA-1(Ab-1) Antibody (ab28839); Right: The same antibody preincubated with synthesized peptide.

All lanes : Anti-GATA1 antibody (ab28839) (1/500-1/1000 dilution)
Lane 1 : extracts from K562 cells (5-30ug).
Lane 2 : extracts from K562 cells (5-30ug).
Predicted band size : 43 kDa
Observed band size : 43 kDa
Western blot analysis of extracts from K562 cells. Line1: Using GATA-1 antibody (ab28839); Line2: The same antibody preincubated with synthesized peptide.

ICC/IF image of ab28839 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 (ab28839, 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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