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Merck
CN

S8689

Fas Ligand, soluble human

recombinant, expressed in HEK 293 cells, lyophilized powder

别名:

SuperFas Ligand

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关于此项目

UNSPSC Code:
12352202
NACRES:
NA.56
MDL number:
Form:
lyophilized powder
Assay:
≥95% (SDS-GE)
Biological source:
human
Recombinant:
expressed in HEK 293 cells
Mol wt:
32 kDa by SDS-PAGE (nonglycosylated form, under reducing conditions)
35 kDa by SDS-PAGE (glycosylated form, under reducing conditions)
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产品名称

Fas Ligand, soluble human, recombinant, expressed in HEK 293 cells, lyophilized powder

biological source

human

recombinant

expressed in HEK 293 cells

assay

≥95% (SDS-GE)

form

lyophilized powder

mol wt

32 kDa by SDS-PAGE (nonglycosylated form, under reducing conditions)
35 kDa by SDS-PAGE (glycosylated form, under reducing conditions)

technique(s)

ligand binding assay: suitable

UniProt accession no.

storage temp.

−20°C

Quality Level

Gene Information

human ... FASLG(356)

Application

ED50 = 1 ng/ml on A20 cells. Does not require any enhancer, as the modified linker sequence already facilitates the formation of active FasL complexes. rhsSuperFas Ligand recognizes its receptor Fas (CD95) of the following species: human, rat, mouse.

Biochem/physiol Actions

Fas ligand has also been shown to be involved in the activation of non-apoptotic pathways including proliferation and NF-κ B activation.
Fas ligand, a protein belonging to the tumor necrosis factor (TNF) family of cytokines, induces apoptosis in cells expressing the cell membrane receptor Fas (CD95/Apo-1).

Legal Information

SuperFas Ligand is a trademark of Alexis Biochemicals Corp.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

Lot/Batch Number

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Harald Wajant et al.
Cytokine & growth factor reviews, 14(1), 53-66 (2002-12-18)
Fas (Apo-1, CD95) and Fas-Ligand (FasL, CD95L) are typical members of the TNF receptor and TNF ligand family, respectively, with a pivotal role in the regulation of apoptotic processes, including activation-induced cell death, T-cell-induced cytotoxicity, immune privilege and tumor surveillance.

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