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Concanavalin A from Canavalia ensiformis (Jack bean), CAS No.11028-71-0

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Concanavalin A from Canavalia ensiformis (Jack bean), CAS No.11028-71-0

5 Citations

COA

Grade & Purity:

Type IV, lyophilized powder

In stock

Item Number

C755208

Grouped product items
SKU	Size	Availability	Price
C755208-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$32.90
C755208-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$80.90
C755208-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$167.90
C755208-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$389.90

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Basic Description

Product Name	Concanavalin A from Canavalia ensiformis (Jack bean), CAS No.11028-71-0
Product Description	Concanavalin A (con A) is a plant lectin refined from jack beans. It is a tetrameric protein, which has four identical 28 kDa subunits. Con A has the ability to connect with the mannose residues of several glycoproteins and can stimulate lymphocytes. Application: Concanavalin A from Canavalia ensiformis (Jack bean) has been used: as T-lymphocyte mitogen in lymphocyte proliferation assay for correlations with organochlorine contaminants (OCs) for in vitro stimulation of T cell hybridomas, BW5147 cells and primary CD4⁺ T cells for T cell vaccination and for induction of hepatitis for the stimulation of mice splenocytes in the suppression of T-lymphocytes proliferation assay for the stimulation of spleen in mitogen assays
Specifications & Purity	Type IV, lyophilized powder
Biochemical and Physiological Mechanisms	Con A is not blood group specific but has an affinity for terminal α-D-mannosyl and α-D-glucosyl residues. Ca2+ and Mn2+ ions are required for activity. Con A dissociates into dimers at pH 5.6 or below. Between pH 5.8 and pH 7.0, Con A exists as a tetrame

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Pyrimidine nucleosides
    - Subclass Pyrimidine 2',3'-dideoxyribonucleosides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Pyrimidine nucleosides
Subclass	Pyrimidine 2',3'-dideoxyribonucleosides
Intermediate Tree Nodes	Not available
Direct Parent	Pyrimidine 2',3'-dideoxyribonucleosides
Alternative Parents	Benzenesulfonamides Benzoic acids Benzenesulfonyl compounds Benzoyl derivatives Pyrimidones Organosulfonamides Hydropyrimidines Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Aminosulfonyl compounds Ureas Lactams Azo imides Azo compounds Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Not available
Substituents	Pyrimidine 2',3'-dideoxyribonucleoside - Benzenesulfonamide - Benzenesulfonyl group - Benzoic acid - Benzoic acid or derivatives - Benzoyl - Pyrimidone - Benzenoid - Organosulfonic acid amide - Pyrimidine - Hydropyrimidine - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous amide - Aminosulfonyl compound - Tetrahydrofuran - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Urea - Lactam - Azo imide - Azo compound - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Storage and Shipping

Concentration	Type IV, lyophilized powder
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads
CAS	11028-71-0

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Mengyuan Chen, Chong Wang, Jing Tan, Jin Wang, Chen Wang. (2025) Cell membrane-inspired COF/AAO hybrid nanofluidic membrane with ion current rectification properties for ultrasensitive detection of E. coli. SENSORS AND ACTUATORS B-CHEMICAL, 423 (136719).
2. Chenze Lu, Gongyan Wang, Xiaoxiao Zhang, Zhihui Fang, Xinyuan Wang, Fan Tang, Kang Ning, Min Xu, Jing Wang, Han Jiang, Ran Tao, Pei Xu. (2025) Cost-effective, label-free electrochemical aptasensors for rapid detection of concanavalin A with screen printed electrodes. FOOD CHEMISTRY, 476 (143338).
3. He Li, Changxin Zheng, Yanru Zheng, Kai Wen, Yingjiu Zhang. (2024) Distinct functional diversity of branched oligosaccharides as chaperones and inhibitory-binding partners of amyloid beta-protein and its aggregates. NEUROPHARMACOLOGY, (110141).
4. Jinming Zhang, Jihang Zhang, Jiale Chen, Xiao Zhang, Jinglan Wu, Pengpeng Yang, Fengxia Zou, Hanjie Ying, Wei Zhuang. (2025) Exploiting unique NP1 interface: Oriented immobilization via electrostatic and affinity interactions in a tailored PDA/PEI microenvironment enhanced by concanavalin A. TALANTA, 286 (127528).
5. Chendi Gao, Ensong Zhang, Xinyu Bian, Qiaoran Li, Chunming Wang, Guang Yang, Ming Jiang, Guosong Chen. (2024) One-Pot Fabrication of Supramolecular Synthetic Protein Hydrogel with Tissue-like Integrated Dynamic Features. BIOMACROMOLECULES, 25 (3): (2065-2074).

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