Key features and details
- Rabbit polyclonal to SI1
- Suitable for: WB, IHC-P
- Reacts with: Human
- Isotype: IgG
Product nameAnti-SI1 antibody
See all SI1 primary antibodies
DescriptionRabbit polyclonal to SI1
Tested applicationsSuitable for: WB, IHC-Pmore details
Species reactivityReacts with: Human
Predicted to work with: Mouse, Rat
Synthetic peptide within Human SI1 aa 398-427 (internal sequence) conjugated to keyhole limpet haemocyanin. The exact sequence is proprietary.
Database link: Q9P2N6
- IHC-P: Human breast tissue. WB: HepG2, MDA-MB-453 and HEK-293 cell lysate.
This product was previously labelled as KIAA1310
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: 0.09% Sodium azide
Concentration information loading...
PurityProtein A purified
Our Abpromise guarantee covers the use of ab230550 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/1000. Predicted molecular weight: 96 kDa.|
|IHC-P||1/100. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.|
- Information by UniProt
- K1310_HUMAN antibody
- KAT8 regulatory NSL complex subunit 3 antibody
- Kiaa1310 antibody
All lanes : Anti-SI1 antibody (ab230550) at 1/1000 dilution
Lane 1 : HepG2 (human liver hepatocellular carcinoma cell line) cell lysate
Lane 2 : MDA-MB-453 cell lysate
Lane 3 : HEK-293 (human epithelial cell line from embryonic kidney) cell lysate
Lysates/proteins at 35 µg per lane.
Developed using the ECL technique.
Predicted band size: 96 kDa
Formalin-fixed, paraffin-embedded human breast tissue stained for SI1 with ab230550 at 1/100 dilution in immunohistochemical analysis.
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
ab230550 has not yet been referenced specifically in any publications.