SAFB Recombinant Monoclonal Antibody, Clone: [5G1], Unconjugated, Rabbit

Catalog Number: CSB-RA018252A0HU
Article Name: SAFB Recombinant Monoclonal Antibody, Clone: [5G1], Unconjugated, Rabbit
Biozol Catalog Number: CSB-RA018252A0HU
Supplier Catalog Number: CSB-RA018252A0HU
Alternative Catalog Number: CSB-RA018252A0HU-100UL, CSB-RA018252A0HU-50UL
Manufacturer: Cusabio
Host: Rabbit
Category: Antikörper
Application: ELISA, FC, IF, IHC, WB
Species Reactivity: Human, Mouse, Rat
Conjugation: Unconjugated
Alternative Names: DKFZp779C1727, glutathione S transferase fusion protein, HAP, HET, HSP27 ERE TATA binding protein, HSP27 ERE-TATA-binding protein, HSP27 estrogen response element-TATA box-binding protein, SAF B, SAF-B, SAF-B1, SAFB 1, SAFB, SAFB1, SAFB1_HUMAN, Scaffold attachment factor B1
Clonality: Monoclonal
Clone Designation: [5G1]
UniProt: Q15424
Buffer: Rabbit IgG in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
Purity: Affinity-chromatography
Form: Liquid
Target: SAFB
Antibody Type: Recombinant Antibody
Application Dilute: Recommended dilution: WB:1:500-1:5000, IHC:1:50-1:200, IF:1:50-1:200, FC:1:50-1:200
Overlay Peak curve showing jurkat cells stained with CSB-RA018252A0HU (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100 for10min. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*106cells) for 45min at 4°C. The secondary antibody used was FITC-conjugated goat anti-rabbit IgG (H+L) at 1/200 dilution for 35min at 4°C.Control antibody (green line) was Rabbit IgG (1ug/1*106cells) used under the same conditions. Acquisition of >10, 000 events was performed.
Immunofluorescence staining of HeLa cell with CSB-RA018252A0HU at 1:50 , counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
IHC image of CSB-RA018252A0HU diluted at 1:100 and staining in paraffin-embedded human small intestine tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.
IHC image of CSB-RA018252A0HU diluted at 1:100 and staining in paraffin-embedded human colorectal cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.
Western Blot
Positive WB detected in: COLO-205 whole cell lysate(30µg), A-431 whole cell lysate(30µg), HEK293 whole cell lysate(30µg), THP-1 whole cell lysate(30µg), Mouse brain tissue lysate(30µg), Rat brain tissue lysate(30µg)
All lanes: SAF B antibody at 1:1000
Secondary
Goat polyclonal to rabbit IgG at 1/40000 dilution
Predicted band size: 103 kDa
Observed band size: 150 kDa
Exposure time:1min