webinar
Oct. 27-28, 2025, Boston, MA, USA - Booth 114.
Read More

BS3 Crosslinker

  CAS No.: 82436-77-9   Cat No.: BADC-01165   Purity: ≥ 97.0 % 4.5  

BS3 Crosslinker is a homobifunctional amine-reactive ADC linker widely used for stable antibody crosslinking and conjugation, enhancing ADC stability and targeted delivery.

BS3 Crosslinker

Structure of 82436-77-9

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C16H20N2O14S2
Molecular Weight
528.47
Shipping
Room temperature
Shipping
Store at -5 °C, keep in dry and avoid sunlight.

* For research and manufacturing use only. We do not sell to patients.

Size Price Stock Quantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

Popular Publications Citing BOC Sciences Products
Synonyms
Bis(sulfosuccinimidyl)suberate
IUPAC Name
1-[8-(2,5-dioxo-3-sulfopyrrolidin-1-yl)oxy-8-oxooctanoyl]oxy-2,5-dioxopyrrolidine-3-sulfonic acid
Canonical SMILES
C1C(C(=O)N(C1=O)OC(=O)CCCCCCC(=O)ON2C(=O)CC(C2=O)S(=O)(=O)O)S(=O)(=O)O
InChI
InChI=1S/C16H20N2O14S2/c19-11-7-9(33(25,26)27)15(23)17(11)31-13(21)5-3-1-2-4-6-14(22)32-18-12(20)8-10(16(18)24)34(28,29)30/h9-10H,1-8H2,(H,25,26,27)(H,28,29,30)
InChIKey
VYLDEYYOISNGST-UHFFFAOYSA-N
Solubility
10 mm in DMSO
Melting Point
>300°C
PSA
255.69000
Appearance
Light tan powder
Shipping
Room temperature
Storage
Store at -5 °C, keep in dry and avoid sunlight.
Pictograms
Irritant
Signal Word
Warning
In Vitro
Treatment of intact cells with the homobifunctional crosslinker BS3 Crosslinker produces similar amounts of covalent dimer in both normal and SAO cells. In SAO cells, copies of normal band 3 can be distinguished from SAO band 3 by treating with H2DIDS to form a crosslink between major chymotryptic fragments (60 kDa and 35 kDa) within one subunit. Successive treatment of cells with [3H]-4,4'-diisothiocyanatodihydrostilbene-2,2'-disulfonate ([3H]H2DIDS), BS3, and chymotrypsin gives 3H-labeled products that include homodimer of normal band 3 as well as products of crosslinking normal band 3 with the 60- and 35-kDa fragment of SAO band 3.

BS3 Crosslinker, a bis(sulfosuccinimidyl) suberate crosslinking reagent, is utilized widely in biochemical research for its non-cleavable and homobifunctional properties. Here are four key applications of BS3 Crosslinker:

Protein-Protein Interaction Studies: In the realm of understanding protein interactions, BS3 Crosslinker plays a pivotal role. By covalently linking interacting proteins together, researchers can stabilize transient complexes, enabling detailed analysis. This innovative technique allows for the detection of interaction partners within intricate biological mixtures, shedding light on complex protein networks.

Structural Biology: Delving into the architecture of proteins within complexes, BS3 Crosslinker is a valuable tool in structural biology. Preceding structural characterization techniques like mass spectrometry or cryo-EM, crosslinking proteins with BS3 provides essential distance constraints for precise 3D modeling. This detailed spatial information enhances our grasp of protein structure and function, offering insights into molecular mechanisms.

Cell Surface Receptor Mapping: With its unique water solubility, BS3 Crosslinker aids in mapping cell surface receptors and their interactions. Capable of permeating the cell membrane without infiltrating intracellular components, this reagent facilitates the crosslinking of surface proteins for in-depth study. By dissecting receptor complexes and signaling pathways crucial for cellular communication, BS3 Crosslinker contributes to unraveling the intricacies of cell signaling.

Antibody-Antigen Complex Analysis: In the realm of immunological studies, BS3 Crosslinker emerges as a critical tool for stabilizing antibody-antigen complexes. By crosslinking these complexes, researchers can analyze binding affinities, map epitopes, and investigate receptor-ligand interactions. This in-depth analysis is instrumental in the development of diagnostic tools and therapeutic antibodies, advancing the field of immunotherapy and precision medicine.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Contact our experts today for pricing and comprehensive details on our ADC offerings.

You May Also Be Interested In

From cytotoxin synthesis to linker design, discover our specialized services that complement your ADC projects.

ADC Linker Development Enzyme Cleavable Linker Cathepsin B Cleavable Linker/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker/Hydrazone Linker

Unlock Deeper ADC Insights

Learn more about payload design, linker strategies, and integrated CDMO support through our curated ADC content.

Linkers - A Crucial Factor in Antibody–Drug Conjugates In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress New Structural Insights Solve Instability Issues of Maleimide Linkers in ADCs PEG Linkers in Antibody-Drug Conjugates Peptide Linkers in Antibody-Drug Conjugates Disulfide Linkers in Antibody-Drug Conjugates Biotinylation Reagents in Antibody-Drug Conjugates Maleimide Linkers in Antibody-Drug Conjugates Current ADC Linker Chemistry SPDB Linkers in Antibody-Drug Conjugates

Explore More ADC Products

Find exactly what your project needs from our expanded range of ADCs, offering flexible options to fit your timelines and goals.

ADC Cytotoxin

Powerful Targeted Cancer Solutions

ADC  Cytotoxin with Linker

Enhanced Stability And Efficacy

ADC Linker

Precise Conjugation For Success

Antibody-Drug  Conjugates (ADCs)

Maximized Therapeutic Performance

Auristatins

Next-Level Tubulin Inhibition

Calicheamicins

High-Impact DNA Targeting

Camptothecins

Advanced Topoisomerase Inhibition

Daunorubicins / Doxorubicins

Trusted Anthracycline Payloads

Duocarmycins

Potent DNA Alkylation Agents

Maytansinoids

Superior Microtubule Disruption

Pyrrolobenzodiazepines

Ultra-Potent DNA Crosslinkers

Traditional Cytotoxic Agents

Proven Chemotherapy Solutions

Cleavable Linker

Precise Intracellular Drug Release

Non-Cleavable Linker

Exceptional Long-Term Stability

Historical Records: BCN-PEG3-VC-PFP ester | PBD dimer | Calicheamicin | Mal-amido-PEG2-Val-Cit-PAB-PNP | MC-Val-Cit-PAB | Mal-PEG4-Val-Cit-PAB-PNP | Azido-PEG3-Val-Cit-PAB-PNP | Amino-PEG6-alcohol | Tisotumab vedotin | Boc-Val-Cit-PABA | BS3 Crosslinker
Send Inquiry
Verification code
Inquiry Basket