Anti-His Tag Rabbit Polyclonal Antibody

SKU:BHA13715040
Overview
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Rabbit polyclonal anti-His Tag antibody validated for WB (1 mg/mL).
Target His Tag
Clonality Polyclonal
Application(s) WB
Host Rabbit
Reactivity Mammals, Bacteria
Options selector
Catalog no. Size
ABT2051-50UL 50 uL
ABT2051-200UL 200 uL
ABT2051-200ULX5 200 uL×5
Available Options
The primary antibody is supplied at 1 mg/mL, this primary antibody is offered in 50 µL, 200 µL, and a value 5 × 200 µL multipack. It is stocked at the manufacturer’s site with an estimated 5–7 business day lead time.
Field Specification
Target His Tag
Alternative names His; 6 His epitope; Hexa His; HHHHHH epitope; Polyhistidine Tag
Host Rabbit
Clonality
  • Polyclonal
Isotype
  • Rabbit IgG
Reactivity
  • Mammals, Bacteria
Applications
  • Western Blot
Immunogen Synthetic Peptide
Purification The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using specific immunogen
Concentration 1 mg/ml
Formulation Liquid solution
Storage 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.
Storage buffer Liquid in PBS, pH 7.4, containing 0.02% Sodium Azide as preservative and 50% Glycerol.
Shipping Gel pack with blue ice.
Catalog no. (Mfr.) ABT2051
Main SKU BHA13715040

Background

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.

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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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