SCAP Antibody (Center)

SKU: orb39255

Description

Peptide affinity purified rabbit polyclonal antibody.

Research Area

Cardiovascular Research, Infectious Disease & Virology, Metabolism Research, Signal Transduction

Images & Validation

• Tested Applications: FC, IF, IHC-P, WB
• Dilution Range: IF - 1:100, WB - 1:2000, IHC-P - 1:50-100, FC - 1:25
• Reactivity: Human, Mouse, Rat
• Predicted Reactivity: Porcine

Key Properties

• Antibody Type: Primary Antibody
• Host: Rabbit
• Clonality: Polyclonal
• Isotype: Rabbit IgG
• Immunogen: Synthetic Peptide
• Target: SCAP
• Molecular Weight: 139729
• Conjugation: Unconjugated

Storage & Handling

• 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
• 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.
• Expiration Date: 12 months from date of receipt.
• Disclaimer: For research use only

Alternative Names

Anti-Sterol regulatory element-binding protein cleavage-activating protein antibody, anti-SREBP cleavage-activating protein antibody, anti-SCAP antibody, anti-PSEC0227 antibody, anti-KIAA0199 antibody, anti-SCAP antibody

Western blot analysis of lysate from PC-3 cell line, using SCAP Antibody (Center). Diluted at 1:1000. A goat anti-rabbit IgG H&L (HRP) at 1:10000 dilution was used as the secondary antibody. Lysate at 35 ug.

Formalin-fixed and paraffin-embedded human colon carcinoma with SCAP Antibody (Center), which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.

Fluorescent confocal image of HeLa cells stained with SCAP (Center) antibody. HeLa cells were fixed with 4% PFA (20 min), permeabilized with Triton X-100 (0.2%, 30 min). Cells were then incubated with SCAP (Center) primary antibody (1:100, 2 h at room temperature). For secondary antibody, Alexa Fluor 488 conjugated donkey anti-rabbit antibody (green) was used (1:1000, 1h). Nuclei were counterstained with Hoechst 33342 (blue) (10 μg/ml, 5 min).

All lanes: Anti-SCAP Antibody (Center) at 1:2000 dilution. Lane 1: Hela whole cell lysate. Lane 2: HT-29 whole cell lysate. Lane 3: K562 whole cell lysate. Lane 4: LNCap whole cell lysate. Lane 5: Mouse brain lysate. Lane 6: Mouse liver lysate. Lane 7: Rat heart lysate. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 140, 98, 96 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

All lanes: Anti-SCAP Antibody (Center) at 1:2000 dilution. Lane 1: Hela whole cell lysate. Lane 2: HT-29 whole cell lysate. Lane 3: K562 whole cell lysate. Lane 4: LNCap whole cell lysate. Lane 5: Mouse brain lysate. Lane 6: Mouse liver lysate. Lane 7: Rat heart lysate. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 140, 98, 96 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

Overlay histogram showing K562 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 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.

Overlay histogram showing K562 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 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.

Quick Database Links

Gene Symbol

SCAP

UniProt

Q12770

RefSeq (Protein):NP_036367.2