Host: Rabbit
Target Protein: RUNX1
Immunogen Range: 101-200/453
Clonality: Polyclonal
Isotype: IgG
Entrez Gene: 861
Source: KLH conjugated synthetic peptide derived from human RUNX1
Purification: Purified by Protein A.
Storage Buffer: 0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
Background:
Size: 100ul
Concentration: 1ug/ul
Applications:
WB(1:300-5000)
ELISA(1:500-1000)
FCM(1:20-100)
IHC-P(1:200-400)
Predicted Molecular Weight: 50
Cross Reactive Species:
Human
Mouse
Predicted Cross Reactive Species:
Rat
Dog
Cow
Horse
Rabbit
For research use only. Not intended for diagnostic or therapeutic use.
- Jinzhu Han. et al. Circ_0027599 elevates RUNX1 expression via sponging miR-21-5p on gastric cancer progression. 2021 May 25Read more>>
- Maggie Lutz. et al. Therapeutic Targeting of the GSK3-CUGBP1 Pathway in Myotonic Dystrophy. INT J MOL SCI. 2023 Jan;24(13):1065Read more>>
Formalin-fixed and paraffin embedded mouse spleen labeled with Rabbit Anti-RUNX1 Polyclonal Antibody, Unconjugated (bs-2744R) at 1:200 followed by conjugation to the secondary antibody and DAB staining\n
Molt4 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with RUNX1 Antibody(bs-2744R)at 1:100 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
Molt4 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with RUNX1 Antibody(bs-2744R)at 1:100 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS, followed by secondary antibody incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).