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Merck
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重要文件

I-042

Supelco

Infliximab solution

certified reference material, ampule of 0.25 mL, Cerilliant®

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About This Item

CAS號碼:
分類程式碼代碼:
41116107
NACRES:
NA.24
暫時無法取得訂價和供貨情況

等級

certified reference material

品質等級

形狀

liquid

特點

Snap-N-Spike®/Snap-N-Shoot®

包裝

ampule of 0.25 mL

製造商/商標名

Cerilliant®

技術

liquid chromatography (LC): suitable

應用

clinical testing

形式

single component solution

儲存溫度

−20°C

一般說明

Infliximab, a purified chimeric IgG monoclonal antibody protein, is created from recombinant DNA technology. It has both mouse and human components to effectively block the activity of tumor necrosis factor-alpha (TNF-α). Infliximab is used to stimulate the immune system of our body and treat certain diseases, including ulcerative colitis, active rheumatoid arthritis, and ankylosing spondylitis.[1]

This product is a certified reference material, consisting of a pure substance within an aqueous solvent solution, 12.5 mM histidine buffer. This standard is prepared and certified under the ISO 17034, ISO/IEC 17025, and ISO 9001 standards, meeting the requirements of a certified reference material and a primary standard per ISO guidelines. This primary standard is suitable to prepare calibrators and/or controls.

應用

Infliximab (Remicade) solution is suitable for analytical and R&D applications for in vitro identification, calibration, and quantification.

特點和優勢

  • Infliximab (Remicade) content is measured via quantitative amino acid analysis (AAA).
  • Ready to use solution.
  • Shelf life and retest date is determined by long term stability studies.
  • The standard is created with precise gravimetric preparation techniques, using fully qualified and calibrated balances that adhere to ISO 17025 standards.
  • The density and material certification are traceable to the SI and higher-order reference materials through mass measurement, calibration, and instrument qualification.
  • The AAA, high-performance liquid chromatography (HPLC) ultraviolet (UV)/mass spectrometry (MS) calibration certified techniques establish traceability.
  • Traceability is ensured to higher order standards from NIST through an unbroken chain of comparisons.

準備報告

  • Thaw contents at either room or refrigerated temperature and mix well prior to usage.
  • Do not refreeze the product after thawing it.
  • Established good laboratory practices should be used when quantitatively transferring the appropriate volume for spiking into a matrix or for dilution purposes.

其他說明

This product′s purpose is for testing. THIS PRODUCT IS NOT INTENDED FOR HUMAN OR THERAPEUTIC USE. Please refer to the safety data sheet for specific information regarding any hazards and appropriate precautions to be taken.

法律資訊

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

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存取文件庫

Infliximab
StatPearls [Internet] (2023)

文章

Learn about the separation of several charge variants of two monoclonal antibodies, NISTmAb and Infliximab, using a polymeric cation exchange column and MS-compatible mobile phases.

Characterize mAb monomers, aggregates, and fragments using SEC-UV workflow with Zenix® and Zenix®-C SEC columns.

Questions

  1. Could you kindly furnish additional details regarding your product, specifically regarding its concentration?

    1 answer
    1. The concentration of Infliximab (Remicade) in Product No. I-042 is listed in the lot-specific Certificate of Analysis. A sample Certificate of Analysis can be found in the Documentation section of the product data page. To obtain the Certificate of Analysis for lots currently in stock, Please contact technical service.

      https://www.sigmaaldrich.com/product/cerillian/i042#product-documentation

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