- Product name
Anti-His Tag Mouse Monoclonal Antibody (5C3)
IF, IP, WB
- Application notes
Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:3000, IF: 1:1000, IP: 1:200.
The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
Fig.1.Immunofluorescence staining (1:2,000) of HA fusion protein in 293 cells with red and counterstained with DAPI.
Fig.2.Western blot analysis of 2ug His fusion protein with Anti-His mouse monoclonal antibody (5C3) in 1:5,000 dilution (lane A) and 1:10,000 dilution (lane B).
Fig.2.IP (1:200) - WB (1:3,000) analysis of His fusion protein expression in 293 cells. Untransfected 293 cell lysate (lane A), transfected 293 cell lysate with His-tag protein (lane B); IP untransfected 293 cell lysate with Anti HA tag mAb (lane C); IP transfected 293 cell lysate with normal Mouse IgG (lane D) or with Anti HA tag mAb (lane E).
- Storage buffer
Liquid in PBS, pH 7.4, containing 0.02% sodium azide as preservative and 50% Glycerol.
- Storage instructions
Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
Gel pack with blue ice.
The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.
A polyhistidine-tag is an amino acid motif in proteins that consists of at least five histidine (His) residues, often at the N- or C-terminus of the protein. It is also known as hexa histidine-tag, 6xHis-tag, and by the trademarked name His-tag. Polyhistidine-tags are often used for affinity purification of polyhistidine-tagged recombinant proteins expressed in Escherichia coli and other prokaryotic expression systems.
- Alternative names
His; 6 His epitope; Hexa His; HHHHHH epitope; Polyhistidine Tag
Most popular with customers
Application: IP, WB
Application: IF, IP, WB
Application: IF, IP, WB
Here we provide some standard research protocols for bioscience including molecular biology, cell biology, immunology, plant biology, genetics, etc. To our knowledge, customized protocols are not required for most products. So please try the standard protocols listed below and let us know how you get on.
Preparation methods for Biochemical
Biochemical reagents have been widely used in life science fundamental research as buffer, probes, substrates, intermediates and standards, etc. You may optimize or choose proper protocols for your specific assay. However, some of tips and suggestions listed below may be for your reference.
Antibody application protocols
Antibodies are useful not only to detect specific biomolecules but also to measure changes in their level and specificity of modification by processes such as phosphorylation, methylation, or glycosylation. Here show some protocols and troubleshooting tips on how to get the best from our antibodies.
- ♦ Antibody Western Blotting (WB) protocol
- ♦ Antibody Immunohistochemistry (IHC) protocol
- ♦ Antibody Immunofluorescence (IF) protocol
- ♦ Antibody Immunoprecipitation (IP) protocol
- ♦ Antibody Enzyme-Linked ImmunoSorbent Assay (ELISA) protocol
Protein&peptide usage suggestions
Synthetic peptides, native or recombinant proteins can be used for medical, academic and research purposes, such as gene therapy, drug screening, antibody production, cell function analysis. Here, we provide some of tips and suggestions for your reference.
- ♦ Handling and storage suggestion for peptides and protein
- ♦ Cytokines and growth factors for cell culture application
Commonly used assay kits guidelines
Assay kits that are simple and convenient to use, which are superior in performance and require little to no time for assay optimization. Further details of specific products which are needed for individual protocols are given in the protocols themselves in booklet.
We hope this will be helpful for your research work. Please let us know through email@example.com if you need more information or support.
An Ultrasensitive Gold Nanoparticle-based Lateral Flow Test for the Detection of Active Botulinum Neurotoxin Type A
Liu J, Gao S, Kang L, et al. Nanoscale Res Lett, 2017, 12(1): 227.
An Asparagine-Rich Protein Nbnrp1 Modulate Verticillium dahliae Protein PevD1-Induced Cell Death and Disease Resistance in Nicotiana benthamiana
Liang Y, Cui S, Tang X, et al. Front Plant Sci, 2018, 7; 9: 303.
MDA5 Induces a Stronger Interferon Response than RIG-I to GCRV Infection through a Mechanism Involving the Phosphorylation and Dimerization of IRF3 and IRF7 in CIK Cells
Wan, Quanyuan, et al. Frontiers in Immunology 8 (2017): 189.
Evidence of VP1 of duck hepatitis A type 1 virus as a target of neutralizing antibodies and involving receptor-binding activity
Li, Xiaojun, et al. Virus Research 227 (2017): 240-244.
Characterization of a C3 Deoxygenation Pathway Reveals a Key Branch Point in Aminoglycoside Biosynthesis
Lv, Meinan, et al. Journal of the American Chemical Society 138.20 (2016): 6427-6435.
Construction of a directional T vector for cloning PCR products and expression in Escherichia coli.
Liang X Y, Liang Z C, Zhang Z, et al. Plasmid, 2015, 79: 15-21.
Combining magnetic nanoparticle with biotinylated nanobodies for rapid and sensitive detection of influenza H3N2.
Zhu M, Hu Y, Li G, et al. Nanoscale research letters, 2014, 9(1): 1.