Product nameAnti-TTC21A/STI2 antibody [EPR17437]
See all TTC21A/STI2 primary antibodies
DescriptionRabbit monoclonal [EPR17437] to TTC21A/STI2
Tested applicationsSuitable for: WBmore details
Species reactivityReacts with: Human
Recombinant fragment within Human TTC21A/STI2 aa 1050 to the C-terminus. The exact sequence is proprietary.
Database link: Q8NDW8
- Human testis lysate.
Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
Storage bufferPreservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol, 0.05% BSA
Concentration information loading...
PurityProtein A purified
Our Abpromise guarantee covers the use of ab201229 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/10000. Detects a band of approximately 150 kDa (predicted molecular weight: 151 kDa).|
Tissue specificityStrongly expressed in testis.
Sequence similaritiesBelongs to the TTC21 family.
Contains 19 TPR repeats.
- Information by UniProt
- STI2 antibody
- Stress-inducible protein 2 antibody
- Tetratricopeptide repeat protein 21A antibody
All lanes : Anti-TTC21A/STI2 antibody [EPR17437] (ab201229) at 1/10000 dilution
Lane 1 : Human testis lysate at 10 µg
Lane 2 : Human cerebellum lysate at 10 µg
Lane 3 : U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) whole cell lysate at 10 µg
Lane 4 : A549 (Human lung carcinoma) whole cell lysate
Lane 5 : Human fetal brain lysate at 10 µg
Lane 6 : Human fetal heart lysate at 10 µg
Lane 7 : Human fetal kidney lysate at 10 µg
Lane 8 : Human fetal spleen lysate at 10 µg
All lanes : Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 151 kDa
Observed band size: 150 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutes
Blocking/Dilution buffer: 5% NFDM/TBST.
ab201229 has not yet been referenced specifically in any publications.