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T9191

Sigma-Aldrich

Anti-TRAIL antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution

Synonym(s):

Anti-Apo-2L

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About This Item

MDL number:
MFCD01868284
UNSPSC Code:
12352203

biological source

rabbit

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen 35 kDa

species reactivity

human

technique(s)

microarray: suitable
western blot: 1 μg/mL using human HeLa cell extract

UniProt accession no.

P50591

shipped in

wet ice

storage temp.

2-8°C

Gene Information

human ... TNFSF10(8743)

Immunogen

synthetic peptide corresponding to amino acids 261-277 of the C-terminal region of human TRAIL (TNF-Related Apoptosis-Inducing Ligand).

Physical form

Supplied as 1.0 mg/ml of IgG fraction of antiserum in phosphate buffered saline containing 0.02% sodium azide

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

12 - Non Combustible Liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificates of Analysis (COA)

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Hanjie Yi et al.
Oncology letters, 16(4), 4768-4772 (2018-09-15)
Non-small cell lung cancer (NSCLC) presents severe threats to the lives of patients. Gefitinib is one of the first-line drugs available for the treatment of NSCLC in the clinical setting. The present study investigated the effects of gefitinib on NSCLC
Ufuk Mert et al.
Cancers, 11(8) (2019-08-17)
Binding of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) to the plasma membrane TRAIL-R1/-R2 selectively kills tumor cells. This discovery led to evaluation of TRAIL-R1/-R2 as targets for anti-cancer therapy, yet the corresponding clinical trials were disappointing. Meanwhile, it emerged that

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