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Anti-6X His tag Recombinant Rabbit Monoclonal Antibody

产品货号 产品 品牌 单位 存货 价格 促销价 数量  
AB-06-5114
Anti-6X His tag Recombinant Rabbit Monoclonal Antibody
洱畔/Erpan Tech 有货

产品特性        

Product Cat#: AB-06-5114
Product type: Primary antibody
Antigen: 6X His tag
Immunogen: Synthetic peptide immune sequence is HHHHHHHHC.
Molecular weight: Predicted band size: – kDa; Observed band size: – kDa
Species immunized: Rabbit
Isotype: IgG
Applications: Western Blot (1:5000-1:10000); Immunoprecipitation (1-2μg/sample); Immunocytochemistry (1:5000-1:10000); Immunohistochemistry-Paraffin (1:5000-1:10000); ELISA (1:10000); Flow Cytometry (1:200-1:500)
Reactivity: Species independent
Clonality (clone number): Monoclonal, PSH07-10
Form: Liquid
Buffer: 1*PBS buffer (pH7.4), 40% glycerol, 0.1% BSA, 0.05% NaN3.
Concentration: 0.2 mg/mL
Purity: Protein A affinity purified
Storage: Aliquot and freeze at -20℃. Avoid multiple freeze/thaw cycles.
Alternative names: 6 His epitope tag antibody
Hexa His tag antibody
HHHHHH epitope tag antibody
HHHHHH tag antibody
His tag antibody
Polyhistidine Tag antibody
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靶标信息

His-Tag Antibody is a high quality monoclonal His-Tag antibody (also designated 6X His-Tag antibody or His-Probe antibody) suitable for the detection of the His-Tag protein. His-Tag Antibody is available as both the non-conjugated anti-His-Tag antibody form, as well as multiple conjugated forms of anti-His-Tag antibody, including agarose, HRP, PE, FITC and multiple Alexa Fluor® conjugates. Plasmid vectors for the expression of coding regions of eukaryotic genes in bacterial, insect and mammalian hosts are in common usage; such expression vectors are frequently used to encode hybrid fusion proteins consisting of a eukaryotic target protein and a specialized region designed to aid in the purification and visualization of the target protein. A system that has proven to be very successful relies on the insertion of a six histidine (His6) sequence in the N-terminus of the encoded protein, allowing for efficient coupling to Ni2+-chelating resins and purification by single step affinity chromatography. This polyhistidine sequence can then be removed by specific cleavage at sites recognized by enzymes such as thrombin or enterokinase, permitting the separation of the target protein from the polyhistidine tag. Visualization of such fusion proteins can be achieved by utilizing antibodies generated against specific peptide sequences downstream from the multiple cloning site.

产品来源

洱畔科技实验室