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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
CHIPseq, WBmore details
Reacts with
Human
Synthetic peptide: K-FPTGPMPPTTSTTVVAPLSS, with N-terminal added Lysine, conjugated to KLH by a Glutaraldehyde linker, corresponding to amino acids 394-413 of Human GATA1.
K-FPTGPMPP TTSTTVVAPL SS
K562 cell line.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 15mM Sodium Azide
Constituents: 1% BSA, 0.01M PBS, pH 7.4
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Immunogen affinity purified
Polyclonal
IgG
Our Abpromise guarantee covers the use of ab11852 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
CHIPseq: Use at an assay dependent concentration. (PubMed: 21795385)
WB: 1/400Detects a band of approximately 45 kDa (predicted molecular weight: 43 kDa).(This concentration is determined using whole extract of K562 human chronic myelogenous leukemia cells. Detects a band of approximately 45 kDa. An additional lower molecular weight band may appear in some preparations. Staining of the GATA1 band is inhibited by the GATA1 peptide (amino acid residues 394-413))
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
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