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Ascentis® Express 90Å C8 (2 μm) HPLC Columns

L × I.D. 5 mm × 3 mm, HPLC Guard Cartridge, pkg of 3 ea

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About This Item

UNSPSC Code:
41115700
NACRES:
SB.52
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Product Name

Ascentis® Express C8, 2 μm Guard Cartridge, 2 μm particle size, L × I.D. 5 mm × 3 mm, pkg of 3 ea

material

stainless steel column

Quality Level

Agency

suitable for USP L7

product line

Ascentis®

feature

endcapped

packaging

pkg of 3 ea

extent of labeling

4.8% carbon loading

technique(s)

HPLC: suitable
LC/MS: suitable
UHPLC-MS: suitable
UHPLC: suitable

L × I.D.

5 mm × 3 mm

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This Item
O7139
antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

conjugate

unconjugated

conjugate

unconjugated

species reactivity

human, rat, chicken, mouse

species reactivity

mouse, rat, chicken, human

biological source

mouse

biological source

mouse

clone

105, monoclonal

clone

O4, monoclonal

technique(s)

flow cytometry: 2.5 μg using using retinoic acid-differentiated NTera-2 human testicular embryonic carcinoma cell line (per 106 cells), immunocytochemistry: 8-25 μg/mL using using NTera-2 human cell line

technique(s)

flow cytometry: 0.25 μg/106 cells (rate differentiated cortical stem cells), immunocytochemistry: 1-10 μg/mL

General description

Ascentis Express Guard Columns provide physical (filtration) and chemical protection for costly analytical columns without compromising the very high performance of Ascentis Express columns. These Ascentis Express guard columns are capable of continuous use at pressures up to 9000 psi (600 bar) with only hand-tightening. Guard cartridges are easily replaced without removing the guard column holder from the flow path. The cartridges are packed with Ascentis Express Fused-Core® particles. Order guard column holder separately.

Legal Information

Ascentis is a registered trademark of Merck KGaA, Darmstadt, Germany
Fused-Core is a registered trademark of Advanced Materials Technology, Inc.

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C M Wen et al.
Journal of fish biology, 90(1), 201-221 (2016-10-13)
In this study, cultures of neural stem-progenitor cells (NSPC) from the brain of green terror cichlid Aequidens rivulatus were established and various NSPCs were demonstrated using immunocytochemistry. All of the NSPCs expressed brain lipid-binding protein, dopamine- and cAMP-regulated neuronal phosphoprotein
Francesca Ruffini et al.
The American journal of pathology, 165(6), 2167-2175 (2004-12-08)
We used expression of the ganglioside A2B5 to isolate putative myelin progenitor cells from adult human central nervous system parenchyma and compared their phenotypic (expression of myelin lineage molecules) and functional (survival, proliferation) properties with mature oligodendrocytes (OLGs) derived from
Nagako Kawashima et al.
Journal of neurochemistry, 111(4), 1031-1041 (2009-09-22)
Sandhoff disease is a progressive neurodegenerative disorder caused by mutations in the HEXB gene which encodes the beta-subunit of N-acetyl-beta-hexosaminidase A and B, resulting in the accumulation of the ganglioside GM2. We isolated astrocytes from the neonatal brain of Sandhoff
C M Wen et al.
Journal of fish biology, 90(1), 201-221 (2016-10-13)
In this study, cultures of neural stem-progenitor cells (NSPC) from the brain of green terror cichlid Aequidens rivulatus were established and various NSPCs were demonstrated using immunocytochemistry. All of the NSPCs expressed brain lipid-binding protein, dopamine- and cAMP-regulated neuronal phosphoprotein
G S Eisenbarth et al.
Proceedings of the National Academy of Sciences of the United States of America, 76(10), 4913-4917 (1979-10-01)
Fusion of spleen cells from a mouse immunized with chicken embryo retina cells with clonal mouse myeloma cells yielded a lymphocyte hybrid cell line that produced antibody that bound to neural tissue such as retina, brain, spinal cord, and dorsal

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