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Product Name 

RUNX1 / AML1 antibody

 

See all RUNX1 / AML1 antibodies (14)...

Product type 

Primary antibodies

Description 

Rabbit polyclonal to RUNX1 / AML1

Immunogen 

Synthetic peptide: PHHPAPTPNPRAS conjugated to BSA, corresponding to C terminal amino acids 213-225 of Human RUNX1 / AML1
BLAST 'PHHPAPTPNPRAS' with BLAST the sequence with ExPASy or BLAST the sequence with NCBI

Reacts with 

Hu, Ms, Rat

Predicted to react 
(species key)

Glla
(Due to sequence homology)

Tested applications 
(see key)

GSA, WB


Abreviews 

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Application notes 
(see key)

Recommended dilutions
GSA: Use at an assay dependent dilution.
WB: 1/200 - 1/1000. Predicted molecular weight: 49 kDa.


Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.

Cellular localization 

Nuclear

Research areas 

Developmental Biology >> Organogenesis >> Hematopoietic system development
Stem Cells >> Hematopoietic Progenitors >> Hemangioblast
Cancer >> Oncoproteins/suppressors >> Oncoproteins >> Transcription factors
Chromatin and Nuclear Signaling >> Chromatin Binding Proteins >> DNA / RNA binding
Stem Cells >> Hematopoietic Progenitors >> Intracellular Molecules
Chromatin and Nuclear Signaling >> Transcription >> Other factors
Neuroscience >> Neurology process >> Neurogenesis

Relevance 

AML1/Runx1 binds DNA as a monomer and through the Runt domain. DNA binding is increased by heterodimerization with CBFB. Isoform AML1L can neither bind DNA nor heterodimerize and interferes with the transactivation activity of AML1/Runx1. CBF binds to the core site, 5'-PYGPYGGT-3', of a number of enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T cell receptor enhancers, LCK, IL3 and GMCSF promoters. The alpha subunit binds DNA and appears to have a role in the development of normal hematopoiesis. AML1/Runx1 is expressed in a wide variety of tissues and is expressed at the highest levels in thymus, bone marrow and peripheral blood. Defects in AML1/Runx1 are the cause of familial platelet disorder with associated myeloid malignancy, an autosomal dominant disease characterized by qualitative and quantitative platelet defects, and propensity to develop acute myelogenous leukemia.

 

Alternative names RUNX1 / AML1 antibody (ab50541)

Database links 

The links below go to external sites and will open in a new browser window

Entrez Gene

    

861    (Human)
12394    (Mouse)
50662    (Rat)

Omim

    

151385    (Human)

SwissProt

    

Q01196    (Human)
Q03347    (Mouse)
Q63046    (Rat)

Unigene

    

612648    (Human)
11201    (Rat)

Raised in 

Rabbit

Clonality 

Polyclonal

Isotype 

IgG

Purity 

Immunogen affinity purified

Storage buffer 

Preservative: None
Constituents: 50% Ammonium sulphate, PBS

Form 

Liquid

Storage instructions 

Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C (add glycerol to a final volume of 50% for extra stability). Avoid repeated freeze / thaw cycles.

 

At Abcam, we have one centralized database to hold all of our product information, so that everything we know about this RUNX1 / AML1 antibody is on this datasheet. But please do contact us if you would like any reassurance!


 

Search PubMed (MEDLINE) for references to RUNX1 / AML1

 

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