GC Antibody (Center)

• Catalog Number: orb1928198
• Category: Antibodies
• Description: Affinity Purified Rabbit Polyclonal Antibody (Pab)
• Target: This GC antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 337-365 amino acids of human GC.
• Clonality: Polyclonal
• Species/Host: Rabbit
• Isotype: Rabbit IgG
• Conjugation: Unconjugated
• Reactivity: Human, Mouse
• Predicted Reactivity: Porcine
• Form/Appearance: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
• UniProt ID: P04062
• MW: 59716 Da
• Tested applications: FC, IHC-P, WB
• Dilution range: WB: 1:2000, WB: 1:1000, IHC-P-Leica: 1:500, FC: 1:25
• Antibody Type: Primary Antibody
• Clone Number: RB21567
• Storage: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
• Alternative names: Glucosylceramidase, Acid beta-glucosidase, Algluce
• Note: For research use only
• NCBI: NP_001005742.1, NP_001005741.1, NP_000148.2

Western blot analysis of GC Antibody (Center) in mouse lung tissue lysates (35 ug/lane). GC (arrow) was detected using the purified Pab.

Immunohistochemical analysis of paraffin-embedded human skeletal muscle tissue was performed on the Leica BOND RXm. Samples were incubated with primary antibody (1/500) for 1 hours at room temperature. A undiluted biotinylated CRF Anti-Polyvalent HRP Polymer antibody was used as the secondary antibody.

All lanes: Anti-GC Antibody (Center) at 1:2000 dilution. Lane 1: 293T/17 whole cell lysate. Lane 2: Hela whole cell lysate. Lane 3: LNCaP whole cell lysate. Lane 4: MCF-7 whole cell lysate. Lane 5: U-2OS whole cell lysate. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 60 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

Overlay histogram showing Hela cells stained (green line). The cells were fixed with 2% paraformaldehyde (10 min) and then permeabilized with 90% methanol for 10 min. The cells were then icubated in 2% bovine serum albumin to block non-specific protein-protein interactions followed by the antibody (1:25 dilution) for 60 min at 37°C. The secondary antibody used was Goat-Anti-Rabbit IgG, DyLight 488 Conjugated Highly Cross-Adsorbed (1583138) at 1/200 dilution for 40 min at 37°C. Isotype control antibody (blue line) was rabbit IgG1 (1 μg/1x10^6 cells) used under the same conditions. Acquisition of > 10000 events was performed.