Host: Rabbit
Target Protein: HOXB4
Immunogen Range: 151-251/251
Clonality: Polyclonal
Isotype: IgG
Entrez Gene: 3214
Swiss Prot: P17483
Source: KLH conjugated synthetic peptide derived from human HOXB4
Purification: Purified by Protein A.
Storage Buffer: 0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage: Shipped at 4C. Store at -20C 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: 28
Cross Reactive Species:
Human
Mouse
Rat
Predicted Cross Reactive Species:
Dog
Sheep
Pig
Chicken
For research use only. Not intended for diagnostic or therapeutic use.
- Emily Honzel. et al. Temporal Expression of Hox Genes and Phox2b in the Rat Nucleus Ambiguus During Development: Implications on Laryngeal Innervation. LARYNGOSCOPE. 2023 JuRead more>>
Paraformaldehyde-fixed, paraffin embedded rat stomach; 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 HOXB4 Polyclonal Antibody, Unconjugated (bs-3650R) at 1:400 overnight at 4°C, followed by a conjugated secondary for 20 minutes and DAB staining.
Lane 1: U87MG cell lysates; Lane 2: Molt-4 cell lysates probed with HOXB4 Polyclonal Antibody, Unconjugated (bs-3650R) at 1:1000 dilution and 4ËšC overnight incubation. Followed by conjugated secondary antibody incubation at 1:20000 for 60 min at 37ËšC.
K562 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 HOXB4 Polyclonal Antibody(bs-3650R)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 incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).
Paraformaldehyde-fixed, paraffin embedded Mouse placenta; 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 HOXB4 Polyclonal Antibody, Unconjugated (bs-3650R) at 1:200 overnight at 4°C, DAB staining.
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 HOXB4 Polyclonal Antibody(bs-3650R)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 incubation for 40 min at room temperature. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).