Lyn Antibodies
We offer Lyn Antibodies for use in common research applications: ELISA, Immunocytochemistry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Paraffin, Immunoprecipitation, Peptide ELISA, Western Blot. Each Lyn Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our Lyn Antibodies can be used in a variety of model species: Chicken, Human, Mouse, Rat. Use the list below to choose the Lyn Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our Lyn polyclonal antibodies and browse our Lyn monoclonal antibody catalog.
Alternate Names for Lyn Antibodies
anti-Lyn antibody, anti-EC 2.7.10 antibody, anti-EC 2.7.10.2 antibody, anti-FLJ26625 antibody, anti-JTK8 antibody, anti-tyrosine-protein kinase Lyn antibody, anti-v-yes-1 Yamaguchi sarcoma viral related oncogene homolog antibody, anti-Yamaguchi sarcoma viral (v-yes-1) related oncogene homolog antibody
12 Results for "lyn" in Primary Antibodies
![Western Blot: Lyn Antibody [NBP2-17188] - A. 30 ug Raji whole cell lysate/extract B. 30 ug K562 whole cell lysate/extract C. 30 ug Raji whole cell lysate/extract 7.5 % SDS-PAGE LYN antibody dilution: 1:1000](http://images.novusbio.com/fullsize/Lyn-Antibody-Western-Blot-NBP2-17188-img0007.jpg "Western Blot: Lyn Antibody [NBP2-17188] - A. 30 ug Raji whole cell lysate/extract B. 30 ug K562 whole cell lysate/extract C. 30 ug Raji whole cell lysate/extract 7.5 % SDS-PAGE LYN antibody dilution: 1:1000")
![Immunocytochemistry/Immunofluorescence: Lyn Antibody [NBP2-17188] - Confocal immunofluorescence analysis of paraformaldehyde-fixed A431, using LYN antibody (Green) at 1:500 dilution. Alpha-tubulin filaments are labeled with Alpha-tubulin antibody (Red) at 1:2000.](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-17188-img0003.jpg)
![Immunohistochemistry-Paraffin: Lyn Antibody [NBP2-17188] - Human colon carcinoma, using LYN antibody at 1:250 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunohistochemistry-Paraffin-NBP2-17188-img0002.jpg)
![Immunoprecipitation: Lyn Antibody [NBP2-17188] - IP samples: K562 whole cell extract A. Control with 4 ug of preimmune Rabbit IgG B. Immunoprecipitation of LYN protein by 4 ug LYN antibody 5 % SDS-PAGE The immunoprecipitated LYN protein was detected by LYN antibody diluted at 1:500. [EasyBlot anti-rabbit IgG was used as a secondary reagent]](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunoprecipitation-NBP2-17188-img0005.jpg)
![Western Blot: Lyn Antibody [NBP2-17188] - Mouse tissue extract (50 ug) was separated by 10% SDS-PAGE, and the membrane was blotted with Lyn antibody (NBP2-17188) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-17188_rabbit-polyclonal-lyn-antibody-910202420122030.jpg)
![<b>Genetic Strategies Validation. </b>Western Blot: Lyn Antibody [NBP2-17188] - Wild-type (WT) and CD44 knockout (KO) HeLa cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with LYN antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-17188_rabbit-polyclonal-lyn-antibody-1610202419405711.jpg)
![Western Blot: Lyn Antibody (LYN-01) [NB500-519] - Fig. 1. Western Blotting analysis (non-reducing conditions) of Lyn using anti-Lyn (LYN-01). Lane 1: negative control Lane 2: RBL rat basophilic leukemia cell line Lane 3: JURKAT human peripheral blood T cell leukemia cell line Lane 4: A-431 human epidermoid carcinoma cell line Lane 5: U-937 human histiocytic lymphoma cell line.](http://images.novusbio.com/fullsize/Lyn-Antibody-LYN-01-Western-Blot-NB500-519-img0001.jpg "Western Blot: Lyn Antibody (LYN-01) [NB500-519] - Fig. 1. Western Blotting analysis (non-reducing conditions) of Lyn using anti-Lyn (LYN-01). Lane 1: negative control Lane 2: RBL rat basophilic leukemia cell line Lane 3: JURKAT human peripheral blood T cell leukemia cell line Lane 4: A-431 human epidermoid carcinoma cell line Lane 5: U-937 human histiocytic lymphoma cell line.")
![Western Blot: Lyn Antibody [NBP1-83072] - Analysis in mouse cell line NIH-3T3 and rat cell line NBT-II.](http://images.novusbio.com/fullsize/Lyn-Antibody-Western-Blot-NBP1-83072-img0008.jpg "Western Blot: Lyn Antibody [NBP1-83072] - Analysis in mouse cell line NIH-3T3 and rat cell line NBT-II.")
![Immunohistochemistry-Paraffin: Lyn Antibody [NBP1-83072] - Staining of human spleen shows high expression.](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunohistochemistry-Paraffin-NBP1-83072-img0010.jpg)
![Western Blot: Lyn Antibody [NBP1-83072] - Analysis in human cell line HELA.](http://images.novusbio.com/fullsize/Lyn-Antibody-Western-Blot-NBP1-83072-img0007.jpg)
![Immunohistochemistry-Paraffin: Lyn Antibody [NBP1-83072] - Staining of human cerebral cortex shows low expression as expected.](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunohistochemistry-Paraffin-NBP1-83072-img0009.jpg)
![<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: Lyn Antibody [NBP1-83072] - Staining in human spleen and cerebral cortex tissues using anti-LYN antibody. Corresponding LYN RNA-seq data are presented for the same tissues.](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunohistochemistry-Paraffin-NBP1-83072-img0011.jpg)
![Western Blot: Lyn Antibody [NBP2-17189] - Sample (30 ug of whole cell lysate) A: NT2D1 7. 5% SDS PAGE gel, diluted at 1:1000.](http://images.novusbio.com/fullsize/Lyn-Antibody-Western-Blot-NBP2-17189-img0001.jpg "Western Blot: Lyn Antibody [NBP2-17189] - Sample (30 ug of whole cell lysate) A: NT2D1 7. 5% SDS PAGE gel, diluted at 1:1000.")
![Immunocytochemistry/Immunofluorescence: Lyn Antibody [NBP2-17189] - Confocal immunofluorescence analysis of paraformaldehyde-fixed A431, using LYN antibody (Green) at 1:500 dilution. Alpha-tubulin filaments are labeled with Alpha-tubulin antibody (Red) at 1:2000.](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunocytochemistry-Immunofluorescence-NBP2-17189-img0002.jpg)
![Immunoprecipitation: Lyn Antibody [NBP2-17189] - K562 whole cell extract A. 40 ug K562 whole cell extract B. Control with 4 ug of preimmune Rabbit IgG C. Immunoprecipitation of LYN protein by 4 ug LYN antibody 5 % SDS-PAGE The immunoprecipitated LYN protein was detected by LYN antibody diluted at 1:500. [EasyBlot anti-rabbit IgG was used as a secondary reagent]](http://images.novusbio.com/fullsize/Lyn-Antibody-Immunoprecipitation-NBP2-17189-img0004.jpg)
![<b>Genetic Strategies Validation. </b>Western Blot: Lyn Antibody [NBP2-17189] - Wild-type (WT) and CD44 knockout (KO) HeLa cell extracts (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with LYN antibody diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.](http://images.novusbio.com/fullsize/nbp2-17189_rabbit-polyclonal-lyn-antibody-1610202419414571.jpg)
![Western Blot: Lyn [p Tyr397] Antibody (HL122) [NBP3-13673] - Untreated (-) and treated (+) Raji whole cell extract (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Lyn (phospho Tyr397) antibody (NBP3-13673) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.](http://images.novusbio.com/fullsize/Lyn-p-Tyr397-Antibody-HL122-Western-Blot-NBP3-13673-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: Lyn [p Tyr397] Antibody (HL122) [NBP3-13673] - Untreated (-) and treated (+) Raji whole cell extract (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Lyn (phospho Tyr397) antibody (NBP3-13673) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody.")
![<b>Biological Strategies Validation. </b>Immunohistochemistry-Paraffin: Lyn [p Tyr397] Antibody (HL122) [NBP3-13673] - Lyn antibody [HL122] detects Lyn protein in the occipital lobe of human Alzheimer's disease brain by immunohistochemical analysis.Sample: Paraffin-embedded Human Matched Pair Tissue Array - Brain (Alzheimer's Disease + Normal) .Lyn stained by Lyn antibody [HL122] (NBP3-13673) diluted at 1:100.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13673_rabbit-lyn-p-tyr-397-mab-hl122-9102024205695.jpg)
![Immunohistochemistry-Paraffin: Lyn [p Tyr397] Antibody (HL122) [NBP3-13673] - Lyn antibody detects Lyn protein by immunohistochemical analysis.Sample: Paraffin-embedded mouse tissues.Lyn stained by Lyn antibody (NBP3-13673) diluted at 1:100.Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](http://images.novusbio.com/fullsize/nbp3-13673_rabbit-lyn-p-tyr-397-mab-hl122-91020242075968.jpg)
![Western Blot: Lyn Antibody (JE44-75) [NBP3-32549] - Western blot analysis of Lyn on different lysates with Rabbit anti-Lyn antibody (NBP3-32549) at 1/1,000 dilution. Lane 1: Ramos cell lysate (15 ug/Lane) Lane 2: A431 cell lysate (15 ug/Lane) Lane 3: Jurkat cell lysate (15 ug/Lane) Lane 4: THP-1 cell lysate (15 ug/Lane) Lane 5: Raji cell lysate (15 ug/Lane) Lane 6: K-562 cell lysate (15 ug/Lane) Lane 7: U-937 cell lysate (15 ug/Lane) Lane 8: Mouse lung tissue lysate (30 ug/Lane) Lane 9: Rat lung tissue lysate (30 ug/Lane) Predicted band size: 59 kDa Observed band size: 55 kDa Exposure time: 30 seconds; 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 (NBP3-32549) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.](http://images.novusbio.com/fullsize/nbp3-32549_rabbit-lyn-mab-je44-75-278202416331240.jpg "Western Blot: Lyn Antibody (JE44-75) [NBP3-32549] - Western blot analysis of Lyn on different lysates with Rabbit anti-Lyn antibody (NBP3-32549) at 1/1,000 dilution. Lane 1: Ramos cell lysate (15 ug/Lane) Lane 2: A431 cell lysate (15 ug/Lane) Lane 3: Jurkat cell lysate (15 ug/Lane) Lane 4: THP-1 cell lysate (15 ug/Lane) Lane 5: Raji cell lysate (15 ug/Lane) Lane 6: K-562 cell lysate (15 ug/Lane) Lane 7: U-937 cell lysate (15 ug/Lane) Lane 8: Mouse lung tissue lysate (30 ug/Lane) Lane 9: Rat lung tissue lysate (30 ug/Lane) Predicted band size: 59 kDa Observed band size: 55 kDa Exposure time: 30 seconds; 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 (NBP3-32549) at 1/1,000 dilution was used in 5% NFDM/TBST at 4 overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.")
![Flow Cytometry: Lyn Antibody (JE44-75) [NBP3-32549] - Flow cytometric analysis of A431 cells labeling Lyn. Cells were fixed and permeabilized. Then stained with the primary antibody (NBP3-32549, 1μg/mL) (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 at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).](http://images.novusbio.com/fullsize/nbp3-32549_rabbit-lyn-mab-je44-75-29202416453275.jpg)
![Western Blot: Lyn [p Tyr 396] Antibody (SR2011) [NBP3-21581] - Western blot analysis using NBP3-21581 in Jurkat cell lysate treated with Pervanadate.](http://images.novusbio.com/fullsize/nbp3-21581_rabbit-lyn-p-tyr-396-mab-sr2011-57202316494241.jpg "Western Blot: Lyn [p Tyr 396] Antibody (SR2011) [NBP3-21581] - Western blot analysis using NBP3-21581 in Jurkat cell lysate treated with Pervanadate.")
![Western Blot: Lyn Antibody [NB100-93453] - (0.1ug/ml) staining of U937 lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.](http://images.novusbio.com/fullsize/Lyn-Antibody-Western-Blot-NB100-93453-img0002.jpg "Western Blot: Lyn Antibody [NB100-93453] - (0.1ug/ml) staining of U937 lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.")
![Western Blot: Lyn [p Tyr396] Antibody (5I5G8) [NBP3-16921] - Western blot analysis of extracts of NIH/3T3 cells, using Lyn Rabbit mAb (NBP3-16921) at 1:1000 dilution.NIH/3T3 cells were treated by pervanadate (1 mM) at 37C for 30 minutes after serum-starvation overnight. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA. Detection: ECL Basic Kit. Exposure time: 30s.](http://images.novusbio.com/fullsize/Lyn-p-Tyr396-Antibody-5I5G8-Western-Blot-NBP3-16921-img0001.jpg "Western Blot: Lyn [p Tyr396] Antibody (5I5G8) [NBP3-16921] - Western blot analysis of extracts of NIH/3T3 cells, using Lyn Rabbit mAb (NBP3-16921) at 1:1000 dilution.NIH/3T3 cells were treated by pervanadate (1 mM) at 37C for 30 minutes after serum-starvation overnight. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% BSA. Detection: ECL Basic Kit. Exposure time: 30s.")
![Western Blot: Lyn [p Tyr397] Antibody [NBP3-12926] - Untreated (-) and treated (+) Raji whole cell extract (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Lyn (phospho Tyr397) antibody (NBP3-12926) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](http://images.novusbio.com/fullsize/Lyn-[p-Tyr397]-Antibody-Western-Blot-NBP3-12926-img0001.jpg "<b>Biological Strategies Validation. </b>Western Blot: Lyn [p Tyr397] Antibody [NBP3-12926] - Untreated (-) and treated (+) Raji whole cell extract (30 ug) were separated by 10% SDS-PAGE, and the membrane was blotted with Lyn (phospho Tyr397) antibody (NBP3-12926) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (NBP2-19301) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.")