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Purified anti-Lck Antibody

Pricing & Availability
Clone
A17013D (See other available formats)
Regulatory Status
RUO
Other Names
Proto-oncogene tyrosine kinase lck, p56-Lck, T-cell specific protein tyrosine kinase
Isotype
Mouse IgG1, κ
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Product Citations
publications
a-A17013D_PURE_Lck_Antibody_1_012518
Total cell lysates (15 μg protein) prepared from HeLa (negative control, Lane 1), Jurkat (Lane 2), or EL4 (Lane 3) cells were resolved by 4-20% Tris-Glycine gel electrophoresis, transferred to nitrocellulose, and probed with 1 μg/mL (1:500 dilution) purified anti-Lck (clone A17013D). Proteins were visualized by chemiluminescence detection using HRP goat anti-mouse-IgG (Cat. No. 405301) at a 1:3000 dilution. Equal loading was confirmed using Direct-Blot™ HRP anti-Actin antibody (Cat. No. 643807) at a 1:5000 dilution. Lane M: MW marker.
  • a-A17013D_PURE_Lck_Antibody_1_012518
    Total cell lysates (15 μg protein) prepared from HeLa (negative control, Lane 1), Jurkat (Lane 2), or EL4 (Lane 3) cells were resolved by 4-20% Tris-Glycine gel electrophoresis, transferred to nitrocellulose, and probed with 1 μg/mL (1:500 dilution) purified anti-Lck (clone A17013D). Proteins were visualized by chemiluminescence detection using HRP goat anti-mouse-IgG (Cat. No. 405301) at a 1:3000 dilution. Equal loading was confirmed using Direct-Blot™ HRP anti-Actin antibody (Cat. No. 643807) at a 1:5000 dilution. Lane M: MW marker.
  • b-A17013D_PURE_Lck_Antibody_2_012518
    Total cell lysates (15 μg protein) prepared from Jurkat cells were resolved by 4-20% Tris-Glycine gel electrophoresis, transferred to nitrocellulose, and probed with the indicated concentration of purified anti-LCK (clones A17013D and LCK-01). Proteins were visualized by chemiluminescence detection using HRP goat anti-mouse-IgG (Cat. No. 405301) at a 1:3000 dilution. Lane M: MW marker.
  • c-A17013D_PURE_Lck_Antibody_4_012518
    Total cell lysates (15 μg protein) prepared from serum starved Jurkat cells treated without (Lane 1) or with (Lane 2) 2 mM H2O2 for 3 minutes were resolved by 4-20% Tris-Glycine gel electrophoresis, transferred to nitrocellulose, and probed with purified anti-Lck Phospho (Tyr505) at 1.0 μg/mL (Cat. No. 684301), purified anti-LCK (clone LCK-01) at 1.0 μg/mL, or purified anti-Lck (Cat. No. 628301) at 1.0 μg/mL. Proteins were visualized by chemiluminescence detection using HRP goat anti-mouse-IgG (Cat. No. 405301) at a 1:3000 dilution. Lane M: MW marker.
  • d-A17013D_PURE_Lck_Antibody_3_012518
    Jurkat cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.5% Triton X-100 for 10 minutes, and blocked with 10% FBS for 60 minutes. Cells were then intracellularly stained with an isotype control antibody at 2.0 μg/mL (1:250 dilution, Panel A), purified anti-Lck clone A17013D at 2.0 µg/mL (1:250 dilution, Panel B) and 1.0 μg/mL (1:500 dilution, Panel C), or purified anti-Lck clone LCK-01 at 2.0 µg/mL (1:250 dilution, Panel D) and 1.0 µg/mL (1:500 dilution, Panel E). Following incubation of all antibodies for two hours at room temperature, cells were incubated with Alexa Fluor® 594 goat anti-mouse IgG (Cat. No. 405308) at 2.0 µg/mL. Nuclei were counterstained with DAPI and the image was captured with a 60X objective.
  • e-A17013D_PURE_Lck_Antibody_5_100119
    Whole cell extracts (250 µg total protein) prepared from Jurkat cells were immunoprecipitated overnight with 2.5 µg of Purified mouse IgG1, κ Isotype Control Antibody (Cat. No. 401401) or Purified anti-Lck Antibody, clone A17013D. The resulting IP fractions and whole cell extract input (6%) were resolved by 4-12% Bis-Tris gel electrophoresis, transferred to a PVDF membrane, and probed with a 1.0 µg/mL (1:500 dilution) of A17013D. Lane M: Molecular Weight marker.
Cat # Size Price Quantity Check Availability Save
601001 25 µg 81€
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601002 100 µg 203€
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Description

Lck is a 56 kD tyrosine protein kinase and a member of the src subfamily that contains both an SH2 and SH3 domain. Alternatively spliced isoforms of Lck have been reported. Lck is a cytoplasmic protein bound to CD4 and CD8 in T lymphocytes that participates in antigen-induced T cell activation through phosphorylation of the T cell receptor zeta chain. Lck is activated upon T cell receptor engagement and is involved in the onset of cell cycle progression induced by interleukin-2. Phosphorylation by Csk downregulates the activity of Lck. In addition to CD4 and CD8, Lck has been reported to interact with PI3K through its SH3 domain and tyrosine phosphorylated KHDRBS1/p70 through its SH2 domain. In addition, Lck has been shown to associate with the SAP transmembrane tyrosine phosphatase.

Product Details
Technical Data Sheet (pdf)

Product Details

Verified Reactivity
Human, Mouse
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
Human Lck peptide phosphorylated around Tyr505.
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography.
Concentration
0.5 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C.
Application

WB - Quality tested
ICC, IP - Verified
Recommended Usage

Each lot of this antibody is quality control tested by Western blotting. For Western blotting, the suggested use of this reagent is 0.25 - 2.0 ug/mL (1:250-2000 dilution) µg per ml. For immunocytochemistry, a concentration range of 1.0 - 2.0 μg/ml (1:100-1:250 dilution) is recommended. For immunoprecipitation, the suggested use of this reagent is 2.5 µg per ml. It is recommended that the reagent be titrated for optimal performance for each application.

Application Notes

Clone A17013D was derived from a human Lck peptide phosphorylated at Y505 immunogen, but still displayed pan reactivity towards the unmodified peptide during western blot screening. This clone was moderately stronger than BioLegend clone LCK-01 for western blot and substantially stronger for immunofluorescence microscopy in parallel testing. But it shows a weak affinity towards mouse Lck. This clone is predicted to recognize both 58 and 61 kD isoforms based off the presence of the immunizing epitope in both proteins and may also recognize certain SRC tyrosine kinase family members due to high sequence similarity.

Phosphorylation of Lck Y505 reduces binding of this antibody by western blot (please see Fig. 3); we recommend LCK-01 as a pan control antibody.

The additional band of ~ 50 kD detected bellow the canonical Lck band in IP experiment could be Lck degradation product.

RRID
AB_2728456 (BioLegend Cat. No. 601001)
AB_2728456 (BioLegend Cat. No. 601002)

Antigen Details

Distribution

Cytoplasmic protein, bound to cytoplasmic CD4 and CD8 in T lymphocytes.

Function
Participates in antigen-induced T cell activation, phosphorylates zeta chain of T cell receptor. Involved in interleukin-2 induced onset of cell cycle progression.
Interaction
Associates with CD4 and CD8 co-receptors. Binds to PI3K through SH3 interactions, binds to tyrosine phosphorylated KHDRBS1/p70 through SH2 domain. Interacts with SAP transmembrane tyrosine phosphatase.
Biology Area
Cell Biology, Signal Transduction, Transcription Factors
Antigen References
  1. Koga Y, et al. 1986. Eur. J. Immunol. 16:1643.
  2. Vogel LB, et al. 1995. Biochem. Biophys. Acta 1264:168.
  3. Vogel LB and Fujita DJ. 1993. Mol. Cell. Biol. 13:7408.
  4. Bergman M, et al. 1992. EMBO J. 11:2919.
Gene ID
3932 View all products for this Gene ID
UniProt
View information about Lck on UniProt.org
Go To Top Version: 2    Revision Date: 10-02-2019

For Research Use Only. Not for diagnostic or therapeutic use.

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms) ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

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This data display is provided for general comparisons between formats.
Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
If you need assistance with selecting the best format contact our expert technical support team.

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