Host: Rabbit
Target Protein: S100A7
Immunogen Range: 41-101/101
Clonality: Polyclonal
Isotype: IgG
Entrez Gene: 6278
Source: KLH conjugated synthetic peptide derived from human S100A7
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:
ELISA(1:500-1000)
FCM(1:20-100)
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: 11
Cross Reactive Species: Human
Predicted Cross Reactive Species:
Cow
Horse
For research use only. Not intended for diagnostic or therapeutic use.
- Yutong Yan. et al. Immunolocalization of antibacterial peptide S100A7 in mastitis goat mammary gland and lipopolysaccharide induces the expression and secretion of S100A7 in goat mammary gland epithelial cells via TLR4/NFB signal pathway. ANIM BIOTECHNOL. 2022 Aug 22Read more>>
- Yutong Yan. et al. The Relationship between Mastitis and Antimicrobial Peptide S100A7 Expression in Dairy Goats. Veterinary Sciences. 2023 Nov;10(11):653Read more>>
K562 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 S100A7 Antibody(bs-6238R)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).
Hela cell; 4% Paraformaldehyde-fixed; Triton X-100 at room temperature for 20 min; Blocking buffer (normal goat serum, C-0005) at 37°C for 20 min; Antibody incubation with (S100A7) polyclonal Antibody, Unconjugated (bs-6238R) 1:100, 90 minutes at 37°C; followed by a conjugated Goat Anti-Rabbit IgG antibody at 37°C for 90 minutes, DAPI (blue, C02-04002) was used to stain the cell nuclei.