Key features and details
- Rabbit polyclonal to SNX15
- Suitable for: IP
- Reacts with: Human
- Isotype: IgG
Product nameAnti-SNX15 antibody
See all SNX15 primary antibodies
DescriptionRabbit polyclonal to SNX15
Tested applicationsSuitable for: IPmore details
Unsuitable for: WB
Species reactivityReacts with: Human
Synthetic peptide within Human SNX15 aa 225-275. The exact sequence is proprietary.
Database link: Q9NRS6
- IP: HEK-293T 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 bufferpH: 6.8
Preservative: 0.09% Sodium azide
Constituents: 0.1% BSA, Tris buffered saline
Concentration information loading...
PurityImmunogen affinity purified
Our Abpromise guarantee covers the use of ab241157 in the following tested applications.
|IP||Use at an assay dependent concentration.
8 - 15 µl/mg lysate
FunctionMay be involved in several stages of intracellular trafficking. Overexpression of SNX15 disrupts the normal trafficking of proteins from the plasma membrane to recycling endosomes or the TGN.
Tissue specificityWidely expressed.
Sequence similaritiesBelongs to the sorting nexin family.
Contains 1 MIT domain.
Contains 1 PX (phox homology) domain.
DomainThe PX domain mediates interaction with membranes enriched in phosphatidylinositol 3-phosphate.
Cellular localizationCytoplasm. Membrane. Cytoplasmic vesicle membrane.
- Information by UniProt
- Clone iota unknown protein antibody
- HSAF001435 antibody
- SNX 15 antibody
SNX15 was immunoprecipitated from HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell lysate (1 mg for IP, 20% of IP loaded) with ab241157 at 8 µl/reaction. Western blot was performed from the immunoprecipitate using ab241157 at 1/1000 dilution.
Lane 1: ab241157 IP in HEK-293T whole cell lysate.
Lane 2: Control IgG IP in HEK-293T whole cell lysate.
Detection: Chemiluminescence with exposure time of 3 minutes.
ab241157 has not yet been referenced specifically in any publications.