推薦產品
product name
BIOshell A400 Protein C4, 3.4 μm HPLC Column, 3.4 μm particle size, L × I.D. 10 cm × 2.1 mm
材料
stainless steel hardware
品質等級
agency
suitable for USP L26
描述
Shell thickness (0.2 μm)
Solid Core (3.0 μm)
產品線
BIOshell
特點
endcapped
製造商/商標名
BIOshell
包裝
1 ea of
標籤範圍
0.4% carbon loading
參數
600 bar max. pressure
90 °C max. temp.
技術
HPLC: suitable
LC/MS: suitable
UHPLC-MS: suitable
UHPLC: suitable
長度 × 內徑
10 cm × 2.1 mm
表面積
15 m2/g
表面覆盖率
4.2 μmol/m2
基質
spherical silica particle platform
superficially porous particle
基質活性組
C4 (butyl) phase
粒徑
3.4 μm
孔徑
400 Å
工作pH值範圍
2-9
分離技術
reversed phase
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文章
-casein basis (electrophoresis), lyophilized powder; β-Casein from bovine milk, BioUltra, ≥98% (PAGE)
BIOshell™ A400 Protein C4 columns contain 3.4 μm particles with 400 Å pores, which are derivatized with dimethylbutyl silane and exhaustively endcapped for optimum protein recovery.
BIOshell™ A400 Protein C4 columns contain 3.4 μm particles with 400 Å pores, which are derivatized with dimethylbutyl silane and exhaustively endcapped for optimum protein recovery.
For use as a marker in SDS-PAGE; Albumin from chicken egg white, For use as a marker in SDS-PAGE; L-Lactic Dehydrogenase from rabbit muscle, Type XI, lyophilized powder, 600-1,200 units/mg protein
條款
Larger porous shell particles with narrow particle size distribution, used in Supelco's BIOshell™ columns for the reversed-phase U/HPLC analysis of peptides and proteins, provide increased efficiency per unit pressure drop.
Optimized USP method for filgrastim, a recombinant form of human granulocyte colony stimulating factor (GCSF). Used in different biologics, it is crucial to know the purity of filgrastim.
HPLC Analysis of the Monoclonal Antibody (mAb) Erbitux (Cetuximab) on BIOshell™ A400 Protein C4
相關內容
HPLC separates and identifies large biomolecules like proteins and peptides by pumping the sample through a sorbent-packed column.
High performance liquid chromatography (HPLC) can be used to separate and identify different large biomolecules such as protein and peptides in a sample. It is based on the pumping of a sample with a solvent (mobile phase) through a column packed with sorbent material (stationary phase) at a high pressure.
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