Anti-HADHA antibody

• Supplier: Abcam
• Catalog: ab54477
• Prices: $400.00
• Sizes: 50 µg
• Host: Rabbit
• Clonality: Polyclonal
• Isotype: IgG
• Applications: IHC-P ICC/IF ICC/IF WB
• Species Reactivities: Mouse, Rat, Human
• Antigen: Synthetic peptide surrounding amino acid 750 (Human)
• Blocking Peptide: HADHA peptide
• Description: Rabbit Polyclonal
• Gene: HADHA
• Conjugate: Unconjugated

Product images

All lanes : Anti-HADHA antibody (ab54477) at 4 µg/mlLane 1 : Jurkat cell lysate 30-50 ug/lane.Lane 2 : Jurkat cell lysate 30-50 ug/lane.Lane 3 : 3T3 cell lysate 30-50 ug/lane.Lane 4 : Rat kidney lysate 30-50 ug/lane.SecondaryAnti-Rabbit IgG, HRP-Linked Antibody at 1/5000 dilution

ICC/IF image of ab54477 stained HepG2 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab54477, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

ab54477 (1µg/ml) staining HADHA in human ileum using an automated system (DAKO Autostainer Plus). Using this protocol there is strong mitochondrial staining.Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.

Product References

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