RUNX1 (phospho Ser249) rabbit pAb

RUNX1 (phospho Ser249) rabbit pAb

AO-06-ES7833-50

RUNX1 (phospho Ser249) rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES7833
Product nameRUNX1 (phospho Ser249) rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameRUNX1; AML1; CBFA2; Runt-related transcription factor 1; Acute myeloid leukemia 1 protein; Core-binding factor subunit alpha-2; CBF-alpha-2; Oncogene AML-1; Polyomavirus enhancer-binding protein 2 alpha B subunit; PEA2-alpha B; PEBP2-alpha
Size50μL
Unit price ($)148
Human gene ID861
Human Swiss-ProtQ01196
SourceRabbit
IsotypeIgG
TargetRUNX1
Fields>>Tight junction;>>Th17 cell differentiation;>>Pathways in cancer;>>Transcriptional misregulation in cancer;>>Chronic myeloid leukemia;>>Acute myeloid leukemia
Gene nameRUNX1
Protein nameRunt-related transcription factor 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID12394
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ03347
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID50662
Rat gene linkView Rat Gene
Rat Swiss-ProtQ63046
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human AML1 around the phosphorylation site of Ser276. AA range:242-291
SpecificityPhospho-RUNX1 (S249) Polyclonal Antibody detects endogenous levels of RUNX1 protein only when phosphorylated at S249.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)49kD
BackgroundCore binding factor (CBF) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters. The protein encoded by this gene represents the alpha subunit of CBF and is thought to be involved in the development of normal hematopoiesis. Chromosomal translocations involving this gene are well-documented and have been associated with several types of leukemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],
Functionalternative products:Additional isoforms seem to exist,caution:The fusion of AML1 with EAP in T-MDS induces a change of reading frame in the latter resulting in 17 AA unrelated to those of EAP.,disease:A chromosomal aberration involving RUNX1/AML1 is a cause of chronic myelogenous leukemia (CML). Translocation t(3;21)(q26;q22) with EAP, MSD1 or EVI1.,disease:A chromosomal aberration involving RUNX1/AML1 is a cause of chronic myelomonocytic leukemia. Inversion inv(21)(q21;q22) with USP16.,disease:A chromosomal aberration involving RUNX1/AML1 is a cause of M2 type acute myeloid leukemia (AML-M2). Translocation t(8;21)(q22;q22) with RUNX1T1/MTG8/ETO.,disease:A chromosomal aberration involving RUNX1/AML1 is a cause of therapy-related myelodysplastic syndrome (T-MDS). Translocation t(3;21)(q26;q22) with EAP, MSD1 or EVI1.,disease:A chromosomal aberration involving RUNX1/AML1 is found in child
Subcellular locationNucleus.
ExpressionExpressed in all tissues examined except brain and heart. Highest levels in thymus, bone marrow and peripheral blood.

Additional Images

Image 1
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Western Blot analysis of Jurkat cells using Phospho-RUNX1 (S249) Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit (SC-003,Inventbiotech,MN,USA).
Image 2
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Western blot analysis of lysates from Jurkat cells, using AML1 (Phospho-Ser276) Antibody. The lane on the right is blocked with the phospho peptide.
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: AO-06-ES7833-50
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