Disease and disorder research has been conducted in relation to the Fatty Acid Elongation Pathway and Tuberculosis, Dehydration, Adrenoleukodystrophy, Malignant Neoplasms, Age Related Macular Degeneration. The study of the Fatty Acid Elongation Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Fatty Acid Elongation Pathway has been researched in relation to Transport, Cell Growth, Fatty Acid Oxidation, Glycolysis, Secretion. The Fatty Acid Elongation Pathway complements our catalog of research reagents including antibodies and ELISA kits against C22, ACACA, ABCD1, FAS, C2.
Top Research Reagents
We have 1945 products for the study of the Fatty Acid Elongation Pathway that can be applied to Chromatin Immunoprecipitation (ChIP), Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
![Western Blot: Fas Receptor/TNFRSF6/CD95 Antibody [NB120-13550] - Fas/TNFRSF6/CD95 Antibody [NB120-13550] - Lane 1: Rat Brain Tissue Extract. Lane 2: Mouse Brain Tissue Extract.](https://images.novusbio.com/fullsize/Fas-TNFRSF6-CD95-Antibody-Western-Blot-NB120-13550-img0007.jpg)
![Immunocytochemistry/Immunofluorescence: Fas Receptor/TNFRSF6/CD95 Antibody [NB120-13550] - Representative IF of cerebellar sections at P10 using an anti-CD95/Fas antibody (green), an anti-calbindin antibody (red) to highlight Purkinje cells. For IF, Hoechst dye (blue) was used to mark nuclei. Scale bar 50 um. Image collected and cropped by CiteAb from the following publication (jneuroinflammation.biomedcentral.com/articles/10.1186/s12974-017-0838-1), licensed under a CC-BY license](https://images.novusbio.com/fullsize/Fas-Receptor-TNFRSF6-CD95-Antibody-Immunocytochemistry-Immunofluorescence-NB120-13550-img0008.jpg)
![Western Blot: ABCB6 Antibody [NBP3-41339] - Sample: Recombinant protein.](https://images.novusbio.com/fullsize/nbp3-41339_rabbit-abcb6-pab-612202421283894.jpg)
![Immunohistochemistry-Paraffin: ABCB6 Antibody [NBP3-41339] - Vector Red staining on IHC-P; Samples: Human Testis Tissue; Primary Ab: 10ug/ml NBP3-41339; Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody](https://images.novusbio.com/fullsize/nbp3-41339_rabbit-abcb6-pab-612202421395378.jpg)
![Western Blot: OXSM Antibody [NBP1-84732] - Lane 1: NIH-3T3 cell lysate (Mouse embryonic fibroblast cells) Lane 2: NBT-II cell lysate (Rat Wistar bladder tumour cells)](https://images.novusbio.com/fullsize/OXSM-Antibody-Western-Blot-NBP1-84732-img0006.jpg)
![Immunohistochemistry-Paraffin: OXSM Antibody [NBP1-84732] - Staining of human lymph node.](https://images.novusbio.com/fullsize/OXSM-Antibody-Immunohistochemistry-Paraffin-NBP1-84732-img0010.jpg)
![Immunohistochemistry-Paraffin: BBS9 Antibody [NBP1-88927] - Staining of human cerebellum shows strong cytoplasmic positivity in purkinje cells.](https://images.novusbio.com/fullsize/BBS9-Antibody-Immunohistochemistry-Paraffin-NBP1-88927-img0002.jpg)
![Western Blot: ELOVL5 Antibody [NBP2-33500] - Analysis in human cell lines U-251MG and MCF-7. Corresponding RNA-seq data are presented for the same cell lines. Loading control: Anti-GAPDH.](https://images.novusbio.com/fullsize/ELOVL5-Antibody-Western-Blot-NBP2-33500-img0011.jpg)
![Immunocytochemistry/Immunofluorescence: ELOVL5 Antibody [NBP2-33500] - Staining of human cell line U-2 OS shows localization to endoplasmic reticulum. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/ELOVL5-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-33500-img0005.jpg)
![Immunocytochemistry/Immunofluorescence: NDUFAB1 Antibody [NBP2-33710] - Staining of human cell line U-2 OS shows localization to mitochondria.](https://images.novusbio.com/fullsize/NDUFAB1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-33710-img0005.jpg)
![Immunohistochemistry-Paraffin: NDUFAB1 Antibody [NBP2-33710] - Staining of human cerebellum shows strong nuclear and cytoplasmic positivity in Purkinje cells.](https://images.novusbio.com/fullsize/NDUFAB1-Antibody-Immunohistochemistry-Paraffin-NBP2-33710-img0001.jpg)
![Western Blot: hnRNP C1 + C2 Antibody (CL2593) [NBP2-36776] - Analysis in U-251MG cells transfected with control siRNA, target specific siRNA probe #1 and #2, using Anti-HNRNPC antibody. Remaining relative intensity is presented. Loading control: Anti-PPIB.](https://images.novusbio.com/fullsize/hnRNP-C1-+-C2-Antibody-CL2593-Western-Blot-NBP2-36776-img0015.jpg)
![Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (CL2593) [NBP2-36776] - Staining in U2OS cell line with Anti-HNRNPC monoclonal antibody, showing distinct nuclear (without nucleoli) staining in green. Microtubule- and nuclear probes are visualized in red and blue respectively (where available). Antibody staining is shown in green.](https://images.novusbio.com/fullsize/hnRNP-C1-+-C2-Antibody-CL2593-Immunocytochemistry-Immunofluorescence-NBP2-36776-img0014.jpg)
![Immunocytochemistry/Immunofluorescence: ELOVL1 Antibody [NBP2-37956] - Staining of human cell line U-2 OS shows localization to endoplasmic reticulum. Antibody staining is shown in green.](https://images.novusbio.com/fullsize/ELOVL1-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-37956-img0004.jpg)
![Immunohistochemistry-Paraffin: ELOVL1 Antibody [NBP2-37956] - Staining in human skin and skeletal muscle tissues . Corresponding ELOVL1 RNA-seq data are presented for the same tissues.](https://images.novusbio.com/fullsize/ELOVL1-Antibody-Immunohistochemistry-Paraffin-NBP2-37956-img0010.jpg)
![Western Blot: FA2H Antibody (OTI2E3) [NBP2-45564] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY FA2H.](https://images.novusbio.com/fullsize/FA2H-Antibody-OTI2E3-Western-Blot-NBP2-45564-img0002.jpg)
![Immunofluorescence: FA2H Antibody (OTI2E3) [NBP2-45564] - Analysis of COS7 cells transiently transfected with pCMV6-ENTRY FA2H.](https://images.novusbio.com/fullsize/FA2H-Antibody-OTI2E3-Immunofluorescence-NBP2-45564-img0001.jpg)
![Western Blot: ABCD1 Antibody (OTI2C12) [NBP2-46476] - Western blot shows lysates of TIME human endothelial parental cell line and ABCD1 knockout (KO) TIME cell line. PVDF membrane was probed with 1:2000 of Mouse Anti-Human ABCD1 Monoclonal Antibody (Catalog # NBP2-46476) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog #HAF018). Specific band was detected for ABCD1 at approximately 75 kDa (as indicated) in the parental TIME cell line, but is not detectable in the knockout TIME cell line. This experiment was conducted under reducing conditions.](https://images.novusbio.com/fullsize/ABCD1-Antibody-OTI2C12-Knockdown-Validated-NBP2-46476-img0005.jpg)
![Western Blot: ABCD1 Antibody (OTI2C12) [NBP2-46476] - Analysis of HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY ABCD1.](https://images.novusbio.com/fullsize/ABCD1-Antibody-OTI2C12-Western-Blot-NBP2-46476-img0004.jpg)
![Western Blot: SREBP1 Antibody (2A4) [NB600-582] - Hepatic SREBP1c and SREBP2 protein abundance in C57BL/6 mice assigned to a high-fat (HF) or a high-fat/exercise (HF + EX) group for 8 weeks. Cytosolic and nuclear SREBP1c abundance. Image collected and cropped by CiteAb from the following publication (https://www.hindawi.com/journals/jl/2013/908048/), licensed under a CC-BY license.](https://images.novusbio.com/fullsize/SREBP1-Antibody-2A4-Western-Blot-NB600-582-img0004.jpg)
![Western Blot: SREBP1 Antibody (2A4) [NB600-582] - Analysis of whole cell lysate from HeLa cells showing a single specific band for the expression of SREBP1 precursor protein (~120 kDa).](https://images.novusbio.com/fullsize/SREBP1-Antibody-2A4-Western-Blot-NB600-582-img0002.jpg)
![Western Blot: Fatty Acid Synthase/FASN Antibody [NB400-114] - Expression of Fatty Acid Synthase in chicken hypothalamus. A: total RNA (1 ug) isolated from different tissues (brain, hypothalamus, liver and muscle) was subjected to RT-PCR using specific primers for chicken Fatty Acid Synthase (GenBank accession JO4485) or ribosomal 18S as a control (GenBank accession AF173612) B: tissue lysates (brain, hypothalmus, liver and muscle) were subjected to Western blot as described in MATERIALS AND METHODS. Blots were incubated with anti-Fatty Acid Synthase antibody and revealed by enhanced chemiluminescence. Picture compliments of Dridi S. et al, Am J Physiol Regul Integr Comp Physiol. 2006 Jul;291(1):R138-47. Epub 2006 Feb 2.](https://images.novusbio.com/fullsize/Fatty-Acid-Synthase-FASN-Antibody-Western-Blot-NB400-114-img0011.jpg)
![Immunocytochemistry/Immunofluorescence: Fatty Acid Synthase/FASN Antibody [NB400-114] - The Fas antibody was tested in MCF-7 cells at a 1:2000 dilution against Dylight 488 (Green). Alpha tubulin and nuclei were counterstained against Dylight 550 (Red) and DAPI (Blue), respectively.](https://images.novusbio.com/fullsize/Fatty-Acid-Synthase-FASN-Antibody-Immunocytochemistry-Immunofluorescence-NB400-114-img0010.jpg)
![Western Blot: ELOVL4 Antibody [NBP3-03895] - Analysis of A-431, using ELOVL4 antibody at 1:400 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit. Exposure time: 180s.](https://images.novusbio.com/fullsize/ELOVL4-Antibody-Western-Blot-NBP3-03895-img0004.jpg)
![Western Blot: ELOVL4 Antibody [NBP3-03895] -analysis of lysates from A-431 cells using ELOVL4 Rabbit pAb at 1:600 dilution.Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25 μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit. Exposure time:30s.](https://images.novusbio.com/fullsize/antibody/nbp3-03895_rabbit-polyclonal-elovl4-antibody-western-blot-4122024101636..png)
![Western Blot: CNBP Antibody - Azide and BSA Free [NBP2-92206] - Western blot analysis of various lysates, using CNBP Rabbit pAb at 1:800 dilution.<br>Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.<br>Lysates/proteins: 25ug per lane.<br>Blocking buffer: 3% nonfat dry milk in TBST.<br>Detection: ECL Basic Kit.<br>Exposure time: 60s.](https://images.novusbio.com/fullsize/nbp2-92206_rabbit-polyclonal-cnbp-antibody-42202514251817.jpg)
![Immunocytochemistry/Immunofluorescence: CNBP Antibody [NBP2-92206] - Analysis of U-2 OS cells using CNBP at dilution of 1:100. Blue: DAPI for nuclear staining.](https://images.novusbio.com/fullsize/CNBP-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-92206-img0001.jpg)
![Western Blot: FEN-1 Antibody (4E7) [NB100-150] - Whole cell extract (30 ug) was separated by 12% SDS-PAGE, and the membrane was blotted with FEN1 antibody diluted at 1:500.](https://images.novusbio.com/fullsize/FEN-1-Antibody-4E7-Western-Blot-NB100-150-img0006.jpg)
![Immunocytochemistry/Immunofluorescence: FEN-1 Antibody (4E7) [NB100-150] - Analysis of paraformaldehyde-fixed MCF7, using antibody at 1:200 dilution.](https://images.novusbio.com/fullsize/FEN-1-Antibody-4E7-Immunocytochemistry-Immunofluorescence-NB100-150-img0004.jpg)
![Flow Cytometry: PPAR alpha/NR1C1 Antibody (3B6/PPAR) [NB300-537] - An intracellular stain was performed on U-87 cells with PPAR alpha/NR1C1 Antibody [3B6/PPAR] NB300-537AF647 (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 2.5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 647.](https://images.novusbio.com/fullsize/PPAR-alpha-NR1C1-Antibody-3B6-PPAR-Flow-Cytometry-NB300-537-img0008.jpg)
![Western Blot: PPAR alpha/NR1C1 Antibody (3B6/PPAR) [NB300-537] - Analysis of 25 ug of Hela (Lane 1), Jurkat (Lane 2), and NIH-3T3 cell lysates (Lane 3) and a molecular weight protein ladder.](https://images.novusbio.com/fullsize/PPAR-alpha-NR1C1-Antibody-3B6-PPAR-Western-Blot-NB300-537-img0006.jpg)