Product Pathways - Lymphocyte Signaling
AML1 (D33G6) XP® Rabbit mAb #4336
|4336S||100 µl (10 western blots)||---||In Stock||---|
|4336P||40 µl (4 western blots)||---||In Stock||---|
|4336||carrier free and custom formulation / quantity||email request|
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Species cross-reactivity is determined by western blot.
Applications Key: W=Western Blotting, IHC-P=Immunohistochemistry (Paraffin), IF-IC=Immunofluorescence (Immunocytochemistry), F=Flow Cytometry
* Product-specific protocol.
Specificity / Sensitivity
AML1 (D33G6) XP® Rabbit mAb detects endogenous levels of total AML1 protein.
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to amino acids at the amino terminus of human AML1.
Western blot analysis of extracts from various cell lines using AML1 (D33G6) XP® Rabbit mAb.
Immunohistochemical analysis of paraffin-embedded human non-Hodgkin's lymphoma using AML1 (D33G6) XP® Rabbit mAb in the presence of control peptide (left) or antigen specific peptide (right).
Flow cytometric analysis of Jurkat cells using AML1 (D33G6) XP® Rabbit mAb (blue) compared to a nonspecific negative control antibody (red).
AML1 (also known as Runx1, CBFA2, and PEBP2αB) is a member of the core binding factor (CBF) family of transcription factors (1,2). It is required for normal development of all hematopoietic lineages (3-5). AML1 forms a heterodimeric DNA binding complex with its partner protein CBFβ and regulates the expression of cellular genes by binding to promoter and enhancer elements. AML1 is commonly translocated in hematopoietic cancers: chromosomal translocations include t(8;21) AML1-ETO, t(12;21) TEL-AML, and t(8;21) AML-M2 (6). Phosphorylation of AML1 on several potential serine and threonine sites, including Ser249, is thought to occur in an Erk-dependent manner (7,8).
- Wang, S. et al. (1993) Mol Cell Biol 13, 3324-3339.
- Ogawa, E. et al. (1993) Proc. Natl. Acad. Sci. USA 90, 6859-6863.
- Okuda, T. et al. (1996) Cell 84, 321-30.
- Wang, Q. et al. (1996) Proc. Natl. Acad. Sci. USA 93, 3444-3449.
- North, T.E. et al. (2004) Stem Cells 22, 158-168.
- Blyth, K. et al. (2005) Nat Rev Cancer 5, 376-387.
- Tanaka, T. et al. (1996) Mol Cell Biol 16, 3967-79.
- Zhang, Y. et al. (2004) J Biol Chem 279, 53116-25.
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For Research Use Only. Not For Use In Diagnostic Procedures.
XP® is a trademark of Cell Signaling Technology, Inc.
Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.