CMP-C9-Biotin-Sialic Acid

R&D Systems | Catalog # ES201

R&D Systems
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Key Product Details

Key Benefits

Species

Multi-Species

Conjugate

Biotin

Product Summary for CMP-C9-Biotin-Sialic Acid

CMP-Azido-Sialic Acid Structure

Formula

C41H65N10O21PS

Molecular Weight

1097.05 Da

Formulation

Lyophilized with Tris, pH 8.0

Stability & Storage

Store the unopened product at < -20 °C. Good for 12 months from date of receipt.

Applications

  • Allow direct biotinylation of sialoglycans of proteins and lipids.
  • Detecting specific sialoglycans on glycoproteins.
  • Detecting and imaging sialoglycans on cells and tissue samples.

Key Features and Benefits:

  • Can be introduced to sialoglycans and glycolipids via various sialyltransferases.
  • Allows glycan imaging on live cells.
  • No side effects on target molecules observed.
  • Convenient and user-friendly.

For Details:

Wu et al. (2015) Carbohydrate Res. 412:1-6.

Wu et al. (2019) Glycobiology, 29:750-754.

Related reagents

Click Chemistry

Enzymes and Detection Reagents for CMP-C9-Biotin-Sialic Acid, ES201

Data Examples

Titration of CMP-C9-Biotin-Sialic Acid on Asialofetuin

Labeling and detection of N-glycans on fetal bovine fetuin
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Labeling and detection of N-glycans on fetal bovine fetuin. Asialofetuin (AF) was prepared from fetal bovine fetuin by treatment with  Recombinant C. perfringens Neuraminidase, CF (Catalog # 5080-NM) and purified through size exclusion chromatography. Asialofetuin (8 µg) was incubated with indicated amounts of CMP-C9-Biotin-Sialic Acid (Catalog # ES201) with constant amount of Recombinant Human ST6GAL1 (aa 44-406) Protein (Catalog # 7620-GT) (0.1 µg) in 25 µl of 25 mM Tris, 10 mM MnCl2, pH7.5 buffer at 37oC for 30 minutes. The reactions were first separated on an SDS-PAGE and imaged by trichloroethylene (TCE) staining (upper panel).  The separated proteins were then blotted to a nitrocellulose membrane and detected with conventional Streptavidin-HRP (Catalog # DY998) chemiluminescence reagents (lower panel).  It is concluded that 0.1 nmol of CMP-C9-Biotin-Sialic Acid will achieve saturating labeling.

Table 1. Enzyme selection for Glycan labeling

Glycans to be labeled Labeling enzymes
(R&D Systems, Catalog# )
Neuraminidase
(R&D Systems, Catalog# )
N-Glycan ST6Gal1 (7620-GT) C. perfringens Neuraminidase (5080-NM)
ST3Gal4
ST3Gal6
O-Glycan ST3Gal1 (6905-GT) C. perfringens Neuraminidase (5080-NM)
ST3Gal2 (7275-GT)
ST6GalNAc1 (9154-GT)
ST6GalNAc2 (6468-GT)
ST6GalNAc3
ST6GalNAc4 (6876-GT)
Polysialic acid (PSA) ST8Sia1 (6716-GT) M. viridifaciens Neuraminidase (5084-NM)
ST8Sia2 (6590-GT)
ST8Sia4 (7027-GT)
ST8Sia6 (9587-GT)
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Formulation, Preparation, and Storage

Shipping

The product is shipped with dry ice or equivalent. Upon receipt, store it immediately at the temperature recommended below.

Storage

Store the unopened product at -20 to -70 °C. Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Do not use past expiration date.

Product Documents for CMP-C9-Biotin-Sialic Acid

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot or batch number in the search box below.

Note: Certificate of Analysis not available for kit components.

Product Specific Notices for CMP-C9-Biotin-Sialic Acid

For research use only

Related Research Areas

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Protocols

View specific protocols for CMP-C9-Biotin-Sialic Acid (ES201):

Sample Protocol for Labeling & Detecting Sialoglycans with Biotinylated Sialic Acid

Protocols are guidelines. Parameters need to be optimized by end users.

Materials

Assay Buffer: 25 mM Tris, 10 mM MnCl2, pH 7.5

Sample glycoprotein

Recombinant sialyltransferases

Recombinant neuraminidase

CMP-C9-Biotin-Sialic Acid (R&D Systems®, Catalog # ES201)

Streptavidin-HRP (R&D Systems®, Catalog # DY998)

SDS-PAGE and Western Blot reagents or equivalent

TBST buffer: 25 mM Tris, 137 mM NaCl, 0.1% Tween-20, pH 7.5

10% Fat Free Milk

Assay Procedure

  1. Prepare reaction mixture by combining a sample glycoprotein (ideally between 1 to 10 µg), 0.5 µg of a recombinant sialyltransferase, 0.1 µg of recombinant neuraminidase, 1 nmol CMP-C9-Biotin-Sialic Acid, in the Assay Buffer with the final volume of 25 μL.
  2. Prepare negative controls by combining a sample glycoprotein (ideally between 1 to 10 µg), 0.1 µg of recombinant neuraminidase, 1 nmol CMP-C9-Biotin-Sialic Acid in the Assay Buffer with the final volume of 25 μL.
  3. Incubate reactions and controls at 37 °C for 30 minutes.
  4. Separate the reactions and controls by SDS-PAGE.
  5. Blot the gel to a nitrocellulose membrane.
  6. Block the blot with 10% fat-free milk for 5 minutes.
  7. Thoroughly wash the membrane with TBST buffer by changing buffer three times for a total of 30 minutes.
  8. Incubate the blot with 25 ng/mL Streptavidin-HRP in 30 mL TBST buffer for 30 minutes.
  9. Thoroughly wash the membrane with TBST buffer by changing buffer three times for a total of 45 minutes.
  10. Detect with commercial ECL (Enhanced Chemiluminescence) reagents.

Final Assay Conditions Per Reaction

CMP-C9-Biotin-Sialic Acid :  1 nmol

Recombinant sialyltransferase:  0.5 µg

Recombinant neuraminidase : 0.1 µg

Sample glycoproteins:  1-10 µg