Anti-His-tag mAb (Trial Size) (Monoclonal Antibody)

Specifications:
Description
For additional information, please see datasheet for standard vial.
Target: | His |
---|---|
Product Type: | Antibody |
Size: | 50 μl |
Application: | FCM, ICC, IP, WB |
Research Area / Disease: | Epitope Tag |
Conjugate: | Unlabeled |
Antibody Type: | Monoclonal |
Clone Number: | OGHis |
Concentration: | 1 mg/mL |
Formulation: | 50 μg IgG in 50 μl volume of PBScontaining 50% glycerol, pH 7.2. No preservative iscontained. |
Isotype: | IgG2a ĸ |
Immunogen: | 6xHis-tagged protein |
Host Species: | Mouse |
Source: | This antibody was purified from hybridoma(clone OGHis) supernatant using protein A agarose. Thishybridoma was established by fusion of mouse myelomacell SP-1 with Balb/c mouse splenocyte immunized with6xHis tagged protein. |
Reactivity: | This antibody recognizes His-taggedprotein on Western blotting, Immunoprecipitation,Immunocytochemistry and Flow cytometry. |
Storage Temperature: | '-20°C |
Regulatory Statement: | For Research Use Only. Not for use in diagnostic procedures. |
Citations
- Hu B et al. HSCARG, a novel regulator of H2A ubiquitination by downregulating PRC1 ubiquitin E3 ligase activity, is essential for cell proliferation. Nucleic Acids Res. 42, 5582-93 (2014),
- Ito M et al. Combinatorial contextualization of peptidic epitopes for enhanced cellular immunity. PLoS One 9, e110425 (2014),
- Kawada J et al. Heteroclitic serological response in esophageal and prostate cancer patients after NY-ESO-1 protein vaccination. Int J Cancer 130, 584-92 (2012),
- Maruyama K et al. ELISA-Based Detection System for Protein S K196E Mutation, a Genetic Risk Factor for Venous Thromboembolism. PLoS One 10, e0133196 (2015),
- Suzuki T et al. Monoubiquitination of Tob/BTG family proteins competes with degradation-targeting polyubiquitination. Biochem Biophys Res Commun. 409, 70-4 (2011),
- Takeiwa T et al. Exportin-5 mediates nuclear export of SRP RNA in vertebrates. Genes Cells 20, 281-91 (2015)
- Cannavo E et al. Regulatory control of DNA end resection by Sae2 phosphorylation. Nat Commun. 9, 4016 (2018)
- Lu X et al. GLP-catalyzed H4K16me1 promotes 53BP1 recruitment to permit DNA damage repair and cell survival. Nucleic Acids Res. 47, 10977-10993 (2019)