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IP10

Protein G Plus/Protein A-Agarose

A mixture of Protein G PLUS and Protein A covalently conjugated to agarose. Useful for purification of IgG from biological fluids.

동의어(들):

Protein G/Agarose

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사이즈/SKU재고 정보가격 (VAT 별도)
10 mL

예상 입고일2026년 9월 28일재고 수량 조회Songdo warehouse

₩1,549,804

제품정보 (DICE 배송 시 비용 별도)

NACRES:
NA.56
UNSPSC Code:
41116133

₩1,549,804


예상 입고일2026년 9월 28일세부사항


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form

slurry (Liquid)

contains

≤0.1% sodium azide as preservative

manufacturer/tradename

Calbiochem®

storage condition

do not freeze

technique(s)

antibody protein purification: suitable, protein purification: suitable

suitability

suitable for microbiology

shipped in

wet ice

storage temp.

2-8°C

General description

A mixture of Protein G PLUS and Protein A covalently conjugated to agarose. Useful for purification of IgG from biological fluids.
Designed for immunoglobulin purification at low pressure. Product size refers to the volume of packed beads.

Application

Antibody Purification

Physical form

50% suspension in PBS.

Other Notes

Note: the product size refers to the volume of packed beads. This product can be used directly with serum, plasma, tissue culture media, ascites, or other biological fluids, but if sufficient quantities of starting material are available we recommend an initial clean up step. The column life will be greatly extended if aggregated proteins and lipids are removed from the immunoglobulin in the clean up step. Use 5-10 ml of packed beads per ml serum.



Recommended Protocol for IgG Purification



Buffers



All concentrations stated are for working solutions, not the 10X concentrates. Caution: sodium azide is poison.



• Binding/Washing Buffer: 100 mM sodium phosphate pH 7.0, 150 mM sodium chloride, 5 mM sodium EDTA, 0.01% sodium azide.

• Elution Buffer A (see Note section): 500 mM ammonium acetate pH 3.0, 0.01% sodium azide.

• Elution Buffer B: 10 mM glycine/HCl pH 3.0, and 0.01% sodium azide.

• Neutralization Buffer: 500 mM Tris Base, 0.01% sodium azide.

• Storage Buffer: 100 mM sodium phosphate, pH 7.0, 0.01% sodium azide.



Protocol



A. Clean Up and Concentration

Ascites and serum should be clotted at room temperature, refrigerated at 4°C overnight (to allow the clot to shrink and lipids to separate), and centrifuged multiple times to remove all clotted protein and lipid. Remove the lipid from the top of the centrifuge tube with a glass rod or small wooden stick. Tissue culture media should be centrifuged or filtered to remove aggregates.

IgG can be concentrated and partially purified by use of an ammonium sulfate precipitation step. Add ammonium sulfate to 50% saturation (313 g per L) with stirring and check the pH adjusting to 7.0 by addition of 1 M HCl or NaOH. Centrifuge to collect precipitated immunoglobulin, dissolve in binding buffer and dialyze against the same buffer.



B. Purification

1. Pack a column with the Agarose Conjugate.

2. Wash with about 20 column volumes Washing/Binding Buffer until pH of eluate is 7.0.

3. If IgG has not been previously dialyzed against binding buffers dilute or dialyze IgG-containing sample into the Washing/Binding Buffer (pH 6.5-7.5).

4. Load sample onto column.

5. Wash with Washing/Binding Buffer until the absorbance of the eluate at 280 nm approaches background level.

6. Wash with Elution Buffer A to elute IgG, and collect fractions until A280 returns to background levels.

7. Wash with Elution Buffer B, and collect fractions until A280 returns to background. Most IgG should elute with buffer A.

8. Neutralize eluted IgG fractions by addition of an equal volume of neutralization buffer and check the pH with pH paper. For best results, neutralize eluate promptly.

9. To re-use the column immediately, repeat procedure from Step 2.

10. To prepare the column for storage, wash column with 5 column volumes of Elution Buffer B.

11. To store column wash with 30 column volumes storage buffer; then seal column outlets and store in refrigerator.

12. Quantitate the purified IgG using the formula:



Absorbance at 280 nm/1.4 = Concentration (mg/ml).



To make Elution Buffer A, start with acetic acid and adjust the pH to 3.0 with ammonium hydroxide.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

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이 품목
IP05E3403LSKMAGAG
description

A mixture of Protein G PLUS and Protein A covalently conjugated to agarose. Useful for purification of IgG from biological fluids.

description

Protein G PLUS/Protein A-Agarose mixture specifically formulated for immunoprecipitation.

description

-

description

The PureProteome Protein A/G Mix Magnetic Bead System provides researchers with the power of the combination of both Protein A and Protein G immunoglobulin binding affinities in one convenient magnetic bead product.

technique(s)

protein purification: suitable

technique(s)

protein purification: suitable

technique(s)

affinity chromatography: suitable, immunoprecipitation (IP): suitable

technique(s)

immunoprecipitation (IP): suitable (crosslinking), protein purification: suitable (antibody)

form

slurry (Liquid)

form

slurry (Liquid)

form

liquid

form

-

suitability

suitable for microbiology

suitability

suitable for microbiology

suitability

-

suitability

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

-

contains

≤0.1% sodium azide as preservative

contains

≤0.1% sodium azide as preservative

contains

-

contains

-

shipped in

wet ice

shipped in

wet ice

shipped in

-

shipped in

wet ice


저장 등급

11 - Combustible Solids

무슨 일이 일어나고 있는 걸까?

WGK 1

인화점 (F)

Not applicable

인화점 (°C)

Not applicable



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