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AB173231

BSA Removal Kit

5

(2 Reviews)

|

(5 Publications)

BSA Removal Kit (ab173231) is designed to remove bovine serum albumin from antibodies that interfere in conjugation/labeling reactions with enzymes or fluorophores.

- Antibody clean up in 10 minutes using one simple step.
- Use on any antibody sub-type and species.
- Compatible with our Lightning-Link® Antibody Conjugation Kits and Oligonucleotide Conjugation Kit range.
1 Images
SDS-PAGE - BSA Removal Kit (AB173231)
  • SDS-PAGE

Supplier Data

SDS-PAGE - BSA Removal Kit (AB173231)

SDS-PAGE Gel showing the use of ab173231 BSA Removal Kit on a mixture containing 1 mg/ml IgG and 1 mg/ml BSA. The gel shows the mix before and after separation. 4-12% Bis-Tris gel, non-reducing.

Key facts

Assay time

10m

Assay type

Direct

Product details

Abcam's BSA Removal Kit (ab173231) is a simple one-step, 10 minute method which effectively separates the BSA from the antibody. The antibody is left in a suitable position for transfer to a buffer more suited to conjugation. The BSA Removal Kit can be used on any antibody sub-type, and species.

This 1 ml kit can remove all of the BSA from up to 1.25 ml of antibody, with a BSA concentration of 0.5% or less. For higher BSA concentrations, the method may need to be repeated, or a higher volume of BSA Removal Buffer may be required.

Please note that this kit is not compatible with our Gold, Latex, Europium and Magnetic Conjugation Kits. To remove BSA from antibodies prior to conjugation with these kits, please use BSA Removal Kit - Nanoparticles (ab204912).

Important considerations:

  • The BSA Removal Kit can separate BSA from antibody solutions with antibody concentrations from 0.03 mg/mL to 10 mg/mL Separation is more efficient at higher antibody concentrations. 50 μg of antibody is the lower limit for seeing a clearly visible pellet.
  • BSA can be effectively separated when present at concentrations of up to 0.5%. If BSA is present at higher concentrations, dilute the antibody mix with de-ionized, distilled water until BSA concentration is 0.5% or less. Alternatively, if BSA is over a 0.5%, two or more runs may need to be performed to completely remove BSA.
  • Glycerol concentration must not exceed 20%.
  • The components of the removal buffer may precipitate at low temperatures. Gently warming the solution should allow solubilisation. Any undissolved crystals should be spun down by brief centrifugation, and the supernatant should be used for the BSA removal.

Abcam's antibody purification and concentration kits offer you a streamlined and efficient solution for isolating and concentrating antibodies from various sources. These kits are designed with simplicity and effectiveness in mind, allowing you to achieve high-purity antibodies with minimal hands-on time. Using our advanced purification technologies, we ensure that your antibodies retain their functionality and specificity, making them ideal for a wide range of applications, including western blotting, immunohistochemistry, and ELISA.

This product is manufactured by Expedeon, an Abcam company, and was previously called AbSelect BSA Removal Kit. 820-0100 is the same as the 1 ml size.

Bovine Serum Albumin (BSA) is often added to purified antibodies as it is an effective stabilizer. However, when labelling antibodies, the BSA becomes a hindrance, as it directly competes with the antibody to attach to the label, greatly reducing the conjugation efficiency. Therefore, prior to undertaking labelling techniques, it is essential to remove the BSA. Common commercial BSA removal techniques can involve many laborious steps.

What's included?

{ "values": { "1mL": { "sellingSize": "1 mL", "publicAssetCode":"ab173231-1mL", "assetComponentDetails": [ { "size":"1 x 500 µL", "name":"Re-suspension Buffer", "number":"AB173231-CMP01", "productcode":"" }, { "size":"1 x 1 mL", "name":"BSA Removal Buffer", "number":"AB173231-CMP02", "productcode":"" } ] } } }

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
+4°C

Product protocols

Target data

Publications (5)

Recent publications for all applications. Explore the full list and refine your search

Nature communications 16:1346 PubMed39905064

2025

Phospho-seq: integrated, multi-modal profiling of intracellular protein dynamics in single cells.

Applications

Unspecified application

Species

Unspecified reactive species

John D Blair,Austin Hartman,Fides Zenk,Philipp Wahle,Giovanna Brancati,Carol Dalgarno,Barbara Treutlein,Rahul Satija

Immunity 57:1696-1709.e10 PubMed38878770

2024

The brain microvasculature is a primary mediator of interferon-α neurotoxicity in human cerebral interferonopathies.

Applications

Unspecified application

Species

Unspecified reactive species

Barney Viengkhou,Emina Hayashida,Sarah McGlasson,Katie Emelianova,Deborah Forbes,Stewart Wiseman,Joanna Wardlaw,Rovin Verdillo,Sarosh R Irani,Darragh Duffy,Fredrik Piehl,Lipin Loo,Axel Pagenstecher,G Greg Neely,Yanick J Crow,Iain L Campbell,David P J Hunt,Markus J Hofer

Journal of the American Heart Association 13:e034990 PubMed38842292

2024

Multiplex Imaging for Cell Phenotyping of Early Human Atherosclerosis.

Applications

Unspecified application

Species

Unspecified reactive species

Maria Elishaev,Boaz Li,Annie Zhou,Kevin Salim,Nicholas J Leeper,Gordon A Francis,Chi Lai,Ying Wang

Nature protocols 16:3802-3835 PubMed34215862

2021

CODEX multiplexed tissue imaging with DNA-conjugated antibodies.

Applications

Unspecified application

Species

Unspecified reactive species

Sarah Black,Darci Phillips,John W Hickey,Julia Kennedy-Darling,Vishal G Venkataraaman,Nikolay Samusik,Yury Goltsev,Christian M Schürch,Garry P Nolan

Nature protocols 13:2121-2148 PubMed30258176

2018

Metal-isotope-tagged monoclonal antibodies for high-dimensional mass cytometry.

Applications

Unspecified application

Species

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Guojun Han,Matthew H Spitzer,Sean C Bendall,Wendy J Fantl,Garry P Nolan
View all publications
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