Anti-Alpha Synuclein SNCA Rabbit Monoclonal Antibody, Clone: [Clone: AGA-19]

Catalog Number: BOB-M00215-1
Article Name: Anti-Alpha Synuclein SNCA Rabbit Monoclonal Antibody, Clone: [Clone: AGA-19]
Biozol Catalog Number: BOB-M00215-1
Supplier Catalog Number: M00215-1
Alternative Catalog Number: BOB-M00215-1-100UL
Manufacturer: Boster Bio
Host: Rabbit
Category: Antikörper
Application: FC, ICC, IF, IHC, IP, WB
Species Reactivity: Human, Mouse, Rat
Immunogen: A synthesized peptide derived from human Alpha Synuclein
Alternative Names: Alpha synuclein, NACP, PARK1, PARK4, SNCA
Boster Bio Anti-Alpha Synuclein SNCA Rabbit Monoclonal Antibody catalog M00215-1. Tested in WB, IHC, ICC/IF, IP, Flow Cytometry applications. This antibody reacts with Human,Mouse,Rat.
Clonality: Monoclonal
Concentration: 0.5mg/ml
Clone Designation: [Clone: AGA-19]
Molecular Weight: Observed Molecular Weight: 30 kDa. Calculated Molecular Weight: 14460 MW
NCBI: 6622
UniProt: P37840
Buffer: Rabbit IgG in stabilizing components, phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. *This antibody is supplied in a stabilized formulation. Compatibility with conjugation reactions depends on the chemistry of the con
Purity: Affinity-chromatography
Form: Liquid
Target: Alpha-synuclein
Application Dilute: WB 1:500-2000IHC 1:50-200ICC/IF 1:50-200IP 1:20FC 1:20
IHC analysis of SNCA using anti-SNCA antibody (M00215-1). SNCA was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog SV0002) with DAB as the chromogen.
IHC analysis of SNCA using anti-SNCA antibody (M00215-1). SNCA was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog SV0002) with DAB as the chromogen.
IHC analysis of SNCA using anti-SNCA antibody (M00215-1). SNCA was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog SV0002) with DAB as the chromogen.
IHC analysis of SNCA using anti-SNCA antibody (M00215-1). SNCA was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M00215-1) overnight at 4C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog SV0002) with DAB as the chromogen.
IHC analysis of SNCA using anti-SNCA antibody (M00215-1). SNCA was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-SNCA Antibody (M0
Western blot analysis of SNCA using anti-SNCA antibody (M00215-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates,Lane 2: human RT4 whole cell lysates,Lane 3: human Hela whole cell lysates.After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNCA antigen affinity purified monoclonal antibody (M00215-1) at 1:500 overnight at 4C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog AR1196-200) with Tanon 5200 system. A specific band was detected for SNCA at approximately 18 kDa. The expected band size for SNCA is at 14 kDa.