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Merck

L5391

Lectin from Bandeiraea simplicifolia (Griffonia simplicifolia)

Isolectin B4 (BSI-B4), peroxidase conjugate, lyophilized powder

Synonyme(s) :

Bandeirea simplicifolia agglutinin, BS-I

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A propos de cet article

NACRES:
NA.32
UNSPSC Code:
12352202
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Nom du produit

Lectin from Bandeiraea simplicifolia (Griffonia simplicifolia), Isolectin B4 (BSI-B4), peroxidase conjugate, lyophilized powder

biological source

Bandieraea simplicifolia

conjugate

peroxidase conjugate

assay

≥90% protein basis (Warburg-Christian)

form

lyophilized powder

potency

<200 μg per mL agglutination activity (using human blood group B erythrocytes)

peroxidase activity

40-160 units/mg protein

composition

Protein, ~95% modified Warburg-Christian

technique(s)

blood typing: suitable
fractionation: suitable

storage temp.

−20°C

Quality Level

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Analysis Note

Agglutination activity is expressed in μg/mL and is determined from serial dilutions of a 1 mg/mL solution using phosphate buffered saline, pH 6.8, containing, for each lectin, calcium, magnesium, and manganese at different concentrations. This activity is the lowest concentration to agglutinate a 2% suspension of appropriate erythrocytes after 1 hr incubation at 25 °C.

Application

General Western Blot Protocol:
  • Glycoprotein sample size: 500ng
  • Lectin Concentration: 0.1ug/ml

  1. Load samples at 500 ng of glycoprotein per lane
  2. Run 4-20% Bis-Tris SDS page gel
  3. Transfer gel to a PVDF membrane
  4. Block membrane for 1 hr at RT with RIPA buffer (R0278 Sigma)
  5. Incubate HRP lectin at 0.1ug/ml with RIPA buffer for 2 hours at RT
  6. Wash membrane 5 x 5 minutes with 25ml RIPA buffer
  7. Detect using chemiluminescent substrate (CPS1-120)

Biochem/physiol Actions

BS-I has a major affinity for terminal α-D-galactosyl residues with a secondary affinity for terminal N-acetyl-α-D-galactosaminyl residues.

Other Notes

BS-I is a tetrameric lectin consisting of two types of subunits designated A and B. There are five BS-I isolectins with different subunit composition: BSI-B4, BSI-AB3, BSI-A2B2, BSI-A3B and BSI-A4. BSI-B4 is blood group B specific and has an exclusive affinity for terminal α-D-galactosyl residues, whereas BSI-A4 has blood group A specificity and has a major affinity for terminal N-acetyl-α-D-galactosaminyl residues.
One unit will form 1 mg purpurogallin in 20 sec from pyrogallol at pH 6.0 at 20 °C.

Physical form

Contains sodium citrate buffer salts and calcium chloride

Preparation Note

Prepared from peroxidase type VI using a modification of the method of O′Sullivan, et al. Repurified by affinity chromatography after conjugation.

Classe de stockage

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Consulter la Bibliothèque de documents

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Hamed Zaer et al.
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Christophe Dubois et al.
Journal of the American College of Cardiology, 55(20), 2232-2243 (2010-05-15)
We compared biological repair after acute myocardial infarction (AMI) with selected porcine progenitor cell populations. Cell types and mechanisms responsible for myocardial repair after AMI remain uncertain. In a blinded, randomized study, we infused autologous late-outgrowth endothelial progenitor cells (EPC)
Hélène Fe Gleitz et al.
EMBO molecular medicine, 10(7) (2018-06-10)
The pediatric lysosomal storage disorder mucopolysaccharidosis type II is caused by mutations in IDS, resulting in accumulation of heparan and dermatan sulfate, causing severe neurodegeneration, skeletal disease, and cardiorespiratory disease. Most patients manifest with cognitive symptoms, which cannot be treated
Jerzy Wiater et al.
International journal of molecular sciences, 22(18) (2021-09-29)
Pig-to-human xenotransplantation seems to be the response to the contemporary shortage of tissue/organ donors. Unfortunately, the phylogenetic distance between pig and human implies hyperacute xenograft rejection. In this study, we tested the hypothesis that combining expression of human α1,2-fucosyltransferase (hFUT2)

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