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RUNX3, mAb (R3-1E10)

 
ALX-803-320-C100 100 µg 350.00 USD
 

Product Specification

Alternative Name:Acute myeloid leukemia 2 protein, Runt-related transcription factor 3, CBF-α3, AML-2, Core-binding factor α3 subunit
 
Clone:R3-1E10
 
Host:Mouse
 
Isotype:IgG1
 
Immunogen:Recombinant human RUNX3 (runt-related transcription factor 3) (aa 191-300).
 
UniProt ID:Q13761
 
Specificity:Recognizes human and mouse RUNX3.
 
Application:Immunohistochemistry (paraffin sections (2µg/ml))
Western Blot (0.2µg/ml)
 
Formulation:Liquid. In PBS containing 0.02% sodium azide.
 
Handling:Avoid freeze/thaw cycles. After opening, prepare aliquots and store at -20°C.
 
Short Term Storage:+4°C
 
Long Term Storage:-20°C
 
Miscellaneous/General:RUNX (Runt-related transcription factor) family members play important roles in normal developmental processes and carcinogenesis. Of the three known RUNX family members, the ubiquitously expressed RUNX3 is involved in neurogenesis, T cell differentiation, tumorigenesis and is a component of the TGF-β induced tumor suppressor pathway. In gastric cancer cells, RUNX3 induces cell cycle arrest and apoptosis through upregulation of Bim, a proapoptotic BH3-only protein. In addition, RUNX3 is frequently inactivated in gastric cancer cells.
 
803-320
Figure 1: Western blot analysis using MAb to RUNX3 (R3-1E10) (Prod. No. ALX-803-320). Method: 0.2µg/ml of MAb to RUNX3 (R3-1E10) were applied to the membrane on which recombinant human (lanes 1-3) or mouse (lanes 4-6) RUNX1, RUNX2 or RUNX3 expressed in COS7 cells were loaded (see [1]).
803-320 ihc
Figure 2: Immunohistochemistry using MAb to RUNX3 (R3-1E10) (Prod. No. ALX-803-320).Method: 2µg/ml of MAb to RUNX3 (R3-1E10) were applied to normal human gastric samples (paraffin sections) which were retrieved by autoclave at 105°C for 15 min. in Dako solution (see [1]).
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803-320 803-320 ihc

Product Literature References

The RUNX3 tumor suppressor upregulates Bim in gastric epithelial cells undergoing transforming growth factor beta-induced apoptosis: T. Yano, et al.; Mol. Cell. Biol. 26, 4474 (2006), Abstract; Full Text

General Literature References

RUNX3 is frequently inactivated by dual mechanisms of protein mislocalization and promoter hypermethylation in breast cancer: Q.C. Lau, et al.; Cancer Res. 66, 6512 (2006), Abstract; Full Text
Tumor suppressor activity of RUNX3: S.C. Bae & J.K. Choi; Oncogene 23, 4336 (2004), Abstract;

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