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00010402

OX-23 hybridoma cell line

Mouse x Mouse Hybridoma,

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About This Item

UNSPSC Code:
41106514
NACRES:
NA.81

Product Name

OX-23 hybridoma cell line, Anti- Factor H, human

biological source

Mouse x Mouse Hybridoma

packaging

tube of 5 μg 00010402-DNA-5UG
pkg of vial of cells 00010402-1VL

ImmunoDon

BALB/c mouse spleen

Myeloma

NS0

Reactivity

Anti-Factor H, human

technique(s)

cell culture | mammalian: suitable

isotype

IgG1

Cell Line Origin

Mouse x Mouse hybridoma

Cell Line Description

The hybridoma line OX-23 was raised by immunizing BALB/c mice with Factor H and fusion of spleen cells with NS0 mouse myeloma cells. The antibody was shown to detect human complement control protein, Factor H. OX-23, also known as MRC OX-23, reduced the increase in cofactor activity observed in the presence of OX-24 (Sigma Catalogue no. 00010403). It was reported that OX-23 and OX-24 react with different epitopes on the Factor H molecule.

Immunogen

Human Factor H

Packaging

NOTE: Both the cell line and DNA from the cell line may be available for this product. Please choose -1VL or VIAL for cells, or -DNA-5UG for DNA.

Culture Medium

RPMI 1640 (R0883) + 2mM Glutamine (G7513) + 10% FBS / FCS (F2442)

Subculture Routine

Maintain cultures between 3-9 x 100,000 cells/ml; 5% CO2; 37°C.

Other Notes

Additional freight & handling charges may be applicable for Asia-Pacific shipments. Please check with your local Customer Service representative for more information.

Disclaimer

This cell line has special release conditions: Commercial organisations are required to complete the ′Cell Line Release Authorisation for Research Use in Commercial Organisations′ release conditions form.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

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Daniel Ajona et al.
Cancer research, 64(17), 6310-6318 (2004-09-03)
The complement system is important in immunosurveillance against tumors. However, malignant cells are usually resistant to complement-mediated lysis. In this study, we examine the expression of factor H, an inhibitor of complement activation, and factor H-like protein 1 (FHL-1), its

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