Anti-FACL4 antibody [EPR8640] - BSA and Azide free
- RabMAb
- Recombinant
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(3 Publications)
Rabbit Recombinant Monoclonal FACL4 antibody. Carrier free. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Human, Mouse, Rat samples. Cited in 3 publications.
View Alternative Names
ACS4, FACL4, LACS4, ACSL4, Long-chain-fatty-acid--CoA ligase 4, Arachidonate--CoA ligase, Long-chain acyl-CoA synthetase 4, LACS 4
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-FACL4 antibody [EPR8640] - BSA and Azide free (AB240135)
Intracellular flow cytometric analysis of permeabilized 293T cells labelling FACL4 with unpurified ab155282 at a dilution of 1/10 (red) compared to a rabbit IgG (negative) (green).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab155282).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-FACL4 antibody [EPR8640] - BSA and Azide free (AB240135)
Immunocytochemistry/Immunofluorescence analysis of HeLa cells labelling FACL4 with purified ab155282 at 1/200. Cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/1000) was used as the secondary antibody. DAPI (blue) was used as the nuclear counterstain. ab7291, a mouse anti-tubulin (1/1000) and ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/1000) were also used.
Control 1 : primary antibody (1/200) and secondary antibody, ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/1000).
Control 2 : ab7291 (1/1000) and secondary antibody, ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/1000).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab155282).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-FACL4 antibody [EPR8640] - BSA and Azide free (AB240135)
Intracellular Flow Cytometry analysis of 293T cells labelling FACL4 with purified ab155282 at 1/100 (red). Cells were fixed with 2% paraformaldehyde. A FITC-conjugated goat anti-rabbit IgG (1/500) was used as the secondary antibody. Black - Isotype control, rabbit monoclonal IgG. Blue - Unlabelled control, cells without incubation with primary and secondary antibodies.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab155282).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FACL4 antibody [EPR8640] - BSA and Azide free (AB240135)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human hepatocellular carcinoma tissue labelling FACL4 with purified ab155282 at 1/200. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. ab97051, a HRP-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/500). Negative control using PBS instead of primary antibody. Counterstained with hematoxylin.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab155282).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FACL4 antibody [EPR8640] - BSA and Azide free (AB240135)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab155282).
Immunohistochemical analysis of formalin fixed paraffin embedded Human liver carcinoma labelling FACL4 with ab155282 at a concentration of 0.5 µg/ml. The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with a OptiView DAB IHC Detection Kit. Heat mediated antigen retrieval was performed with DISCOVERY cell conditioning solution (CC1) 100°C, pH8.5 for 32mins.
ab155282 anti FACL4 antibody EPR8640 was incubated for 16mins at 37°C. Sections were counterstained with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.
Customers are encouraged to optimise antigen retrieval conditions, antibody concentration, incubation times and temperature for best results in their own IHC assay workflow (automated and manual)
- IP
Lab
Immunoprecipitation - Anti-FACL4 antibody [EPR8640] - BSA and Azide free (AB240135)
ab155282 (purified) at 1/30 immunoprecipitating FACL4 in HepG2 whole cell lysate.
Lane 1 (input) : HepG2 whole cell lysate (10µg)
Lane 2 (+) : ab155282 + HepG2 whole cell lysate.
Lane 3 (-) : Rabbit monoclonal IgG (ab172730) instead of ab155282 in HepG2 whole cell lysate.
For western blotting, a HRP-conjugated anti-rabbit IgG, specific to the non-reduced form of IgG was used as the secondary antibody (1/1500).
Blocking buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM /TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab155282).
All lanes:
Immunoprecipitation - Anti-FACL4 antibody [EPR8640] (<a href='/en-us/products/primary-antibodies/facl4-antibody-epr8640-ab155282'>ab155282</a>)
Predicted band size: 79 kDa
Observed band size: 79 kDa
false
- WB
Lab
Western blot - Anti-FACL4 antibody [EPR8640] - BSA and Azide free (AB240135)
This data was developed using ab155282, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/1000000 dilution.
Smear bands above the 79 kDa position is acceptable, as FACL4 contains multiple ubiquitination sites.
All lanes:
Western blot - Anti-FACL4 antibody [EPR8640] (<a href='/en-us/products/primary-antibodies/facl4-antibody-epr8640-ab155282'>ab155282</a>) at 1/1000 dilution
Lane 1:
Human brainstem tissue lysate at 20 µg
Lane 2:
SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Mouse brain tissue lysate at 20 µg
Lane 4:
Mouse heart tissue lysate at 20 µg
Lane 5:
Mouse kidney tissue lysate at 20 µg
Lane 6:
Rat brain tissue lysate at 20 µg
Lane 7:
Rat heart tissue lysate at 20 µg
Lane 8:
Rat kidney tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 79 kDa
false
Exposure time: 100s
Related conjugates and formulations (8)
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Anti-FACL4 antibody [EPR8640]
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660 APC
APC Anti-FACL4 antibody [EPR8640]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-FACL4 antibody [EPR8640]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-FACL4 antibody [EPR8640]
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-FACL4 antibody [EPR8640]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-FACL4 antibody [EPR8640]
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HRP Anti-FACL4 antibody [EPR8640]
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578 PE
PE Anti-FACL4 antibody [EPR8640]
Reactivity data
Product details
ab240135 is the carrier-free version of ab155282.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
FACL4 contributes significantly to lipid metabolism and is involved in the synthesis of complex lipids. It facilitates the integration of long-chain fatty acids into phospholipids and triglycerides. FACL4 often functions as part of larger lipid synthesis and modification complexes working closely with other enzymes to maintain membrane integrity and signal transduction. Its activity influences cellular responses to changes in lipid availability and metabolic demands.
Pathways
FACL4 functions within the arachidonic acid metabolism and glycerophospholipid metabolic pathways. In these pathways other proteins such as COX and LOX interact with FACL4 to regulate inflammatory responses and membrane lipid composition. The enzyme’s role in these pathways highlights its contribution to managing the balance between pro-inflammatory and anti-inflammatory metabolites which are essential for cell signaling and homeostasis.
Product protocols
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Target data
Publications (3)
Recent publications for all applications. Explore the full list and refine your search
Methods in molecular biology (Clifton, N.J.) 2712:157-163 PubMed37578704
2023
Applications
Unspecified application
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Unspecified reactive species
Andrology 11:332-343 PubMed36098277
2022
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Unspecified reactive species
Molecular medicine reports 19:4761-4769 PubMed30957190
2019
Applications
Unspecified application
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Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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