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Ankyron TNF11_HUMAN Clone AE40109
Clone Information
|
Clone ?
|
AE40109 |
|
Gene
|
TNFSF11 OPGL RANKL TRANCE |
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UniProtID
|
O14788 |
|
Organism
|
Homo sapiens (Human) |
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Entry Name
|
TNF11_HUMAN |
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SNR ?
|
760 |
|
Product Type
|
Monomer |
|
Ankyron Applications
|
F, IF, IHC, ELISA, WB |
|
Pack Size
|
100ug |
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Label ?
Clones are also labelled with a His tag by default
|
Ankyrons® Testing Data
Lymphocytes were fixed in formaldehyde (1%), then stained using 1.4 µg V5-tagged Ankyron and anti-V5 antibody conjugated with APC (red) in Permeabilisation Staining Buffer (RPMI 1640 + 10 % human serum + 0.5% saponin), counterstaining nuclei with DAPI (blue). Inset: negative control of anti-V5 APC antibody alone.
Lymphocytes were fixed in formaldehyde (1%), then stained using 1.4 µg V5-tagged Ankyron and anti-V5 APC (red) in Permeabilisation Staining Buffer (RPMI 1640 + 10 % human serum + 0.5% saponin), counterstaining nuclei with DAPI (blue).
Immunohistochemical analysis of paraffin-embedded human spleen using 10 μg/ml V5-tagged Ankyron and anti-V5 HRP (1 in 500), detecting with DAB (brown) and counterstaining nuclei with haematoxylin (blue-purple). Heat-mediated antigen retrieval with Leica Tris-EDTA buffer (pH9).
Flow cytometric analysis of human lymphocytes following fixation with formaldehyde (1%) and subsequent co-incubation of 0.4 μg of Ankyron with anti-V5 APC (red). Negative control, anti-V5 APC only (grey).
Flow cytometric analysis of human lymphocytes following permeabilization and staining with pre-conjugated Ankyron (0.4 µg) and anti-V5 APC (red). Negative control, anti-V5 APC only (grey).
Colorimetric western blot analysis of purified target protein (1µg - 10 ng) using 1 µg/ml V5-tagged Ankyron preconjugated with anti-V5-HRP (1 in 500).
Binding assay determination of the signal to noise ratio (SNR) of V5-labeled Ankyrons® AE40109 binding to 0.5 picomoles of immobilised TNF11_HUMAN, over a background (BG) of non-cognate target protein. The Ankyron was pre-conjugated with the ProImmune Anti-V5 HRP label reagent before detection with a chemiluminescence substrate.