Anti-GST antibody (ab19256)
Key features and details
- Rabbit polyclonal to GST
- Suitable for: ICC/IF, ELISA, WB, IP
- Reacts with: Species independent
- Isotype: IgG
Overview
-
Product name
Anti-GST antibody
See all GST primary antibodies -
Description
Rabbit polyclonal to GST -
Host species
Rabbit -
Tested applications
Suitable for: ICC/IF, ELISA, WB, IPmore details -
Species reactivity
Reacts with: Species independent -
Immunogen
Glutathione-S-Transferase (GST) from Schistosoma japonicum.
Properties
-
Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle. -
Storage buffer
pH: 6.8
Preservative: 0.1% Sodium azide
Constituent: PBS -
Concentration information loading... -
Purity
Immunogen affinity purified -
Clonality
Polyclonal -
Isotype
IgG -
Research areas
Images
-
Western blot - Anti-GST antibody (ab19256)All lanes : Anti-GST antibody (ab19256) at 1/15000 dilution
Lane 1 : HEK293 lysate at 0.1 µg
Lane 2 : HEK293 lysate at 0.3 µg
Lane 3 : HEK293 lysate at 1 µg
Predicted band size: 24 kDa
Exposure time: 3 secondsDetected by Chemiluminescence.
-
Western blot - Anti-GST antibody (ab19256) This image is courtesy of an Abreview submitted by Dr Hanneke OkkenhaugAll lanes : Anti-GST antibody (ab19256) at 1/5000 dilution
Lane 1 : GST tagged purified protein from E. Coli BL21 cells at 0.1 µg
Lane 2 : GST tagged purified protein from E. Coli BL21 cells at 0.2 µg
Lane 3 : GST tagged purified protein from E. Coli BL21 cells at 0.4 µg
Secondary
All lanes : A HRP conjugated donkey polyclonal to rabbit at 1/10000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 24 kDa
Observed band size: 72 kDa why is the actual band size different from the predicted?
Exposure time: 5 seconds
-
Immunocytochemistry/ Immunofluorescence - Anti-GST antibody (ab19256) Image from Joset A et al, J Cell Biol 188:271-85 (2010), Fig 5.NogoΔ20-induced Rho activation depends on internalization. (A–C) Rho activation levels were examined in PC12 cells that were either untreated (control; A), treated with 300 nM NogoΔ20 for 30 min at 37°C in absence of mutant PincherG68E (B), or treated with 300 nm NogoΔ20 treated for 30 min at 37°C in the presence of mutant PincherG68E (C). Active GTP-bound Rho was detected by incubation with GST-tagged Rhotekin-RBD and immunostaining using ab19256. Bar, 20 µm. (D) Densitometric quantification of staining from three independent experiments. Data are normalized to the mean of the untreated group ± SEM (error bars); asterisks marks highly significant differences between untreated, NogoΔ20-treated, or NogoΔ20- and dn PincherG68E-treated cells (three experiments; 30–50 cells per experiment; ***, P
