Host: Rabbit
Target Protein: S100P binding protein
Immunogen Range: 331-408/408
Clonality: Polyclonal
Isotype: IgG
Entrez Gene: 64766
Swiss Prot: Q96BU1
Source: KLH conjugated synthetic peptide derived from human S100P binding protein
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: 46
Cross Reactive Species:
Human
Mouse
Predicted Cross Reactive Species: Rat
For research use only. Not intended for diagnostic or therapeutic use.
- Mo, Jing, et al. "The in-vitro spheroid culture induces a more highly differentiated but tumorigenic population from melanoma cell lines." Melanoma Research (2013).Read more>>
- Yu Chen. et al. Effect of necrostatin-1 on sciatic nerve crush injury in rat models. J ORTHOP SURG RES. 2023 Dec;18(1):1-9Read more>>
Lane 1: Mouse Spleen cell lysates; Lane 2: Mouse Lung cell lysates probed with S100P binding protein Polyclonal Antibody, Unconjugated (bs-6577R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.
Lane 1: Molt-4 cell lysates; Lane 2: Mouse Cerebellum cell lysates probed with S100P binding protein Polyclonal Antibody, Unconjugated (bs-6577R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C.
Mouse spleen cells(black) 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 S100P binding protein Polyclonal Antibody(bs-6577R)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2% BSA in PBS, followed by secondary antibody(blue) incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
K562 cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 0.1% ice-cold methanol for 20 min at room temperature, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with S100P binding protein Antibody(bs-6577R)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).