Host: Rabbit
Target Protein: Bcl-2 Ser70
Modification Site: Ser70
Clonality: Polyclonal
Isotype: IgG
Entrez Gene: 24224
Swiss Prot: P49950
Source: KLH conjugated synthetic phosphopeptide derived from rat Bcl-2 around the phosphorylation site of Ser70
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)
IHC-F(1:100-500)
IF(IHC-P)(1:50-200)
IF(IHC-F)(1:50-200)
IF(ICC)(1:50-200)
Predicted Molecular Weight: 26
Cross Reactive Species:
Human
Mouse
Rat
Predicted Cross Reactive Species:
Dog
Rabbit
For research use only. Not intended for diagnostic or therapeutic use.
- Yan, Jia-Qing, et al. "Overexpression of Human E46K Mutant α-Synuclein Impairs Macroautophagy via Inactivation of JNK1-Bcl-2 Pathway." Molecular Neurobiology (2014): 1-17.Read more>>
- Shuyu Fang. et al. All-trans-retinoic acid inhibits the malignant behaviors of hepatocarcinoma cells by regulating autophagy. Am J Transl Res. 2020; 12(10): 6793C681Read more>>
Formalin-fixed and paraffin embedded rat kidney labeled with Rabbit Anti Phospho-Bcl-2(Ser70) Polyclonal Antibody, Unconjugated (bs-3052R) at 1:200 followed by conjugation to the secondary antibody and DAB staining
Mouse spleen lysates probed with Anti-Bcl-2 (Ser70) Polyclonal Antibody, Unconjugated (bs-3052R) at 1:300 in 4˚C. Followed by conjugation to secondary antibody (bs-0295G-HRP) at 1:5000 90min in RT
Image submitted by OWL Validation Program. 20 μg proteins of cell lysates from A431, U266 and THP-1 were separated by SDS-PAGE and transferred to PVDF membrane for western blotting analysis antibodies against bs-3052r Rabbit Anti-Bcl-2 (Ser70) Polyclonal Antibody at dilution of 1:1000 with exposure time of 10 min.
Paraformaldehyde-fixed, paraffin embedded Human pancreatic cancer; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with Bcl-2 (Ser70) Polyclonal Antibody, Unconjugated (bs-3052R) at 1:200 overnight at 4°C, DAB staining.
HL-60 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 0.1% PBST for 20 min at room temperature, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with Bcl-2 (Ser70) Polyclonal Antibody(bs-3052R)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).