Host: Rabbit
Target Protein: NFIB/NF1B2
Immunogen Range: 1-100/420
Clonality: Polyclonal
Isotype: IgG
Source: KLH conjugated synthetic peptide derived from human NFIB/NF1B2
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)
ICC(1:100-500)
Predicted Molecular Weight: 47
Cross Reactive Species:
Human
Mouse
Predicted Cross Reactive Species:
Rat
Cow
Sheep
Pig
Chicken
Rabbit
For research use only. Not intended for diagnostic or therapeutic use.
- Hanyue Ying. et al. CircATL2 enhances paclitaxel resistance of ovarian cancer via impacting miR-506-3p/NFIB axis. 2021 Sep 19Read more>>
293T lysates probed with NFIB Polyclonal Antibody, Unconjugated (bs-11899R) at 1:300 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:10000 for 60 min at 37˚C.
Mouse Brain lysates probed with NFIB Polyclonal Antibody, Unconjugated (bs-11899R) at 1:300 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:10000 for 60 min at 37˚C.
Lane 1: Human Hela cell lysates; Lane 2: Human A431 cell lysates; Lane 3: Mouse Lung lysates; Lane 4: Mouse Ovary lysates; Lane 5: Mouse Kidney lysates probed with NFIB/NF1B2 Polyclonal Antibody, Unconjugated (bs-11899R) at 1:1000 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37˚C
A431 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 NFIB/NF1B2 Polyclonal Antibody(bs-11899R)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).