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Merck

H9890

Sigma-Aldrich

羟基磷灰石 制备

40% (by weight), aqueous ethanol suspension, 60-180 μm

别名:

Hydroxyapatite preparation

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About This Item

MDL號碼:
分類程式碼代碼:
12352200

形狀

aqueous ethanol suspension

濃度

40% (by weight)

粒徑

60-180 μm

pH值

4-13

儲存溫度

2-8°C

應用

HA ultrogel is used in affinity chromatography, protein chromatography and adsorption/partition.

其他說明

Microcrystalline hydroxyapatite in cross-linked 4% beaded agarose

外觀

Suspension in 1 M NaCl containing 20% ethanol

法律資訊

Ultrogel is a registered trademark of Pall Corporation

象形圖

Flame

訊號詞

Warning

危險聲明

危險分類

Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

104.0 °F

閃點(°C)

40 °C


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S A Kim et al.
Applied and environmental microbiology, 63(9), 3432-3437 (2006-03-15)
To investigate why Rhizobium sp. (Cicer) strain CC 1192 cells accumulate poly-R-3-hydroxybutyrate in the free-living state but not as bacteroids in nodules on chickpea (Cicer arietinum L.) plants, we have examined the kinetic properties of acetyl coenzyme A (acetyl-CoA) acetyltransferase
Purification and characterization of the acid lipase from the endosperm of castor oil seeds.
Fuchs, C., et al.
Journal of Plant Physiology, 149(1-2), 23-29 (1996)
P Borowski et al.
The Biochemical journal, 331 ( Pt 2), 649-657 (1998-06-11)
The catalytic domain of p72(syk) kinase (CDp72(syk)) was purified from a 30000 g particulate fraction of rat spleen. The purification procedure employed sequential chromatography on columns of DEAE-Sephacel and Superdex-200, and elution from HA-Ultrogel by chloride. The analysis of the
H S Lee et al.
Plant physiology, 112(4), 1513-1522 (1996-12-01)
Neutral and alkaline invertase were identified in cells of a suspension culture of carrot (Daucus carota L.) and purified to electrophoretic homogeneity. Neutral invertase is an octamer with a molecular mass of 456 kD and subunits of 57 kD, whereas
Sung-Woon Hong et al.
European journal of biochemistry, 270(15), 3168-3173 (2003-07-19)
Salt-active acharan sulfate lyase (no EC number) has been purified from Bacteroides stercoris HJ-15, which was isolated from human intestinal bacteria with GAG degrading enzymes. The enzyme was purified to apparent homogeneity by a combination of QAE-cellulose, diethylaminoethyl (DEAE)-cellulose, CM-Sephadex

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