DIA-900 – Anti-HIS Epitope-Tag (rec) from Mouse (Clone: 13/45/31) – unconj. – 200 µg

Art.-Nr.
DIA-900

Specificity
6-His Epitop-Tag
His-tag (N/C-terminal)
HIS Epitope-Tag
Species Reactivity
all
recombinant
Host Species
Mouse
Isotype
IgG1
Clone
13/45/31
Clonality (Mono-/Polyclonal)
monoclonal
Application
Immunohistochemistry (frozen sections)
Immunofluorescence
Flow Cytometry
Western Blot
Immunohistochemistry (IHC)
Conjugation
unconjugated
Format
ProteinA/G purified (from culture supernatant)
Peptide
DIA 900 inkl. 6-His-Protein
Positive Control
5 µg rec. (His)6-p53 Prot. für SDS-PAGE included
Product line / Topic
Epitope-Tags, Haptens and Label
Intended Use
for Research Use Only
Temperature – Storage
2-8°C
Search Code
DIA900
histag
histidin tag
anti his
hexahistidine
his6
6his
polyhistidine
histidine
Manufacturer / Brand
dianova

Reactivity

The mouse monoclonal anti-(His)6-tag antibody, clone 13/45/31-2 (H. Zentgraf/DKFZ Heidelberg, Germany), specifically detects any kind of histidine-tagged proteins in cells and complex cellular lysates. This monoclonal antibody specifically reacts with recombinant proteins containing an epitope of at least 6 histidine residues, located at the N-terminus, C-terminus or at both termini. A higher number of histidine residues leads to an increased binding affinity of the antibody, e.g. an expression product with 10 histidine residues increases the affinity about 10- to 20-fold. In most cases additional flanking amino acids aren’t required for antibody binding, therefore enabling the choice of many different expression vectors on the only condition that the epitope is spatially available.

Background

Recombinant proteins are utilized for various purposes in molecular biology such as the production of antibodies for investigation of the mechanism of protein-nucleic acid or protein-protein interactions. Many prokaryotic expression vectors have been established enabling synthesis of the protein of interest as a fusion with a peptide, thus facilitating purification. Expression of recombinant proteins in E. coli as a fusion protein with neighbouring histidine residues is one of the most popular methods, because the proteins have useful attributes. The affinity of the histidine-tag motif to Ni2+ by chelation is strong and selective enough to enable purification of the protein to homogeneity by affinity chromatography on a Ni2+-NTA adsorbant.

Western blot detection (WB) with anti-HIS Epitope-Tag Antibody (clone 13/45/31) -dianova

Detection of (HIS)6-p53 Hela cell lysates (Transfection with HIS-tagged protein vector, SDS-PAGE and western blotting according to standard procedures). Sensitivity: Specific detection of 1ng protein in 8μg total proteins at a 1:100 antibody dilution / Antibody di-lutions up to 1:10.000 for less sensitive detections (ca. 6ng HIS-tagged protein).

References:

1. Zentgraf H, Frey M, Schwinn S, Tessmer C, Willemann B, Samstag Y, Velhagen I. Detection of histidine-tagged fusion pro-teins by using a high-specific mouse monoclonal anti-histidine tag antibody. Nucleic Acids Res.16,3347-8, 1995.