Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, FC, IF-Cell |
Clonality: | Monoclonal |
Clone number: | JE58-56 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 62 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human COASY aa 510-564. |
Positive control: | HepG2 cell lysate, HeLa cell lysate, A431 cell lysate, HepG2. |
Subcellular location: | Mitochondrion matrix, Cytoplasm. |
Recommended Dilutions:
WB FC IF-Cell |
1:1,000-1:2,000 1:1,000 1:100 |
Uniprot #: | SwissProt: Q13057 Human |
Alternative names: | Bifunctional coenzyme A synthase Bifunctional phosphopantetheine adenylyl transferase/dephospho CoA kinase CoA synthase COASY COASY_HUMAN Coenzyme A synthase Dephospho-CoA kinase Dephospho-CoA pyrophosphorylase Dephosphocoenzyme A kinase DPCK DPCOAK NBP Nucleotide binding protein Pantetheine-phosphate adenylyltransferase Phosphopantetheine adenylyltransferase / dephosphocoenzyme A kinase pOV 2 POV-2 POV2 PPAT UKR1 |
Fig1:
Western blot analysis of COASY on different lysates with Rabbit anti-COASY antibody (HA721128) at 1/1,000 dilution. Lane 1: HAP1-parental cell lysate Lane 2: HAP1-COASY KD cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 62 kDa Observed band size: 62 kDa Exposure time: 120 seconds; ECL: K1801; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721128) at 1/1,000 dilution was used in K1803 at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Western blot analysis of COASY on different lysates with Rabbit anti-COASY antibody (HA721128) at 1/2,000 dilution. Lane 1: HepG2 cell lysate Lane 2: HeLa cell lysate Lane 3: A431 cell lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 62 kDa Observed band size: 62 kDa Exposure time: 25 seconds; ECL: K1801; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721128) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
Fig3:
Flow cytometric analysis of HepG2 cells labeling COASY. Cells were fixed and permeabilized. Then stained with the primary antibody (HA721128, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |
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Fig4:
Immunocytochemistry analysis of HepG2 cells labeling COASY with Rabbit anti-COASY antibody (HA721128) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-COASY antibody (HA721128) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Counterstained with Mitotracker. Nuclear DNA was labelled in blue with DAPI. |