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ab31810 |
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Read our guarantee »Products:Tags & Cell Markers >> Subcellular Markers >> Organelles >> ER
Anti-PDI antibody - ER Marker
See all PDI products (10) ...
Rabbit polyclonal to PDI - ER Marker
IHC-P, WB, ICC/IFmore details
Reacts with
Mouse, Rat, Human
Predicted to work with
Chicken, Cow
Synthetic peptide conjugated to KLH derived from within residues 400 - 500 of Human PDI.
(Peptide available as ab31810.)
This antibody gave a positive signal in the lysates: Human Brain Whole Tissue Lysate, Human Kidney Whole Tissue Lysate, Human Liver Whole Tissue Lysate and Human Testes Whole Tissue Lysate, Mouse Liver Whole Tissue Lysate; Rat Liver Whole Tissue Lysate.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 1% BSA, PBS. pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Cancer >> Cancer Metabolism >> Response to hypoxia
Tags & Cell Markers >> Subcellular Markers >> Organelles >> ER
Our Abpromise guarantee covers the use of ab31811 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: 1/800Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
WB: Use a concentration of 1 µg/mlDetects a band of approximately 57 kDa (predicted molecular weight: 57 kDa).
ICC/IF: Use a concentration of 1 µg/ml
Acts as an intracellular estrogen-binding protein. May be involved in modulating cellular levels and biological functions of estrogens in the pancreas. May act as a chaperone that inhibits aggregation of misfolded proteins.
Highly expressed in pancreas (at protein level).
Belongs to the protein disulfide isomerase family.
Contains 2 thioredoxin domains.
The disulfide-linked homodimer exhibits an enhanced chaperone activity.
Glycosylated.
Endoplasmic reticulum lumen.
Target information above from: UniProt accessionQ13087
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - PDI antibody (ab31811)

All lanes : Anti-PDI antibody - ER Marker (ab31811) at 1 µg/ml
Lane 1 : Human Brain Whole Tissue Lysate
Lane 2 : Human Kidney Whole Tissue Lysate at 20 µg
Lane 3 : Human Liver Whole Tissue Lysate at 20 µg
Lane 4 : Human Testes Whole Tissue Lysate at 20 µg
Secondary
IR Dye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/15000 dilution
Performed under reducing conditions.
Predicted band size : 57 kDa
Observed band size : 57 kDa
Several smaller bands are seen in Human Liver Whole Tissue Lysate. These are predicted to be break-down products of PDI; the banding pattern is consistent with that observed in Liver lysates for other available PDI antibodies.
- PDI antibody - ER Marker (ab31811)

Image courtesy of Human Protein Atlas
ab31811 staining PDI in Human gall bladder. The paraffin embedded tissue was incubated with ab31811 (1/800 dilution) for 30 mins at room temperature. Antigen retrieval was performed by heat induction in citrate buffer pH 6. ab31811 was tested in a tissue microarray (TMA) containing a wide range of normal and cancer tissues as well as a cell microarray consisting of a range of commonly used, well characterised human cell lines.
Further results for this antibody can be found at www.proteinatlas.org
Immunocytochemistry/ Immunofluorescence - PDI antibody - ER Marker (ab31811)

ICC/IF image of ab31811 stained human HEK 293 cells. The cells were 4% PFA fixed (10 min), permabilised in 0.1% PBS-Tween (20 min) and incubated with the antibody (ab31811, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue). This antibody also gave a positive IF result in HeLa and MCF7 cells.
Western blot - PDI antibody - ER Marker (ab31811)

All lanes : Anti-PDI antibody - ER Marker (ab31811) at 1 µg/ml
Lane 1 : Liver (Mouse) Tissue Lysate
Lane 2 : Liver (Rat) Tissue Lysate
Lysates/proteins at 10 µg per lane.
Secondary
Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP), pre-adsorbed (ab97080) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 57 kDa
Observed band size : 57 kDa
Exposure time : 30 seconds
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PDI antibody - ER Marker (ab31811)

IHC image of ab31811 staining in pancreas formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab31811, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
ab31811 has not yet been referenced specifically in any publications.
Publishing research using ab31811? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
Find concentration of your lot:

All lanes : Anti-PDI antibody - ER Marker (ab31811) at 1 µg/ml
Lane 1 : Human Brain Whole Tissue Lysate
Lane 2 : Human Kidney Whole Tissue Lysate at 20 µg
Lane 3 : Human Liver Whole Tissue Lysate at 20 µg
Lane 4 : Human Testes Whole Tissue Lysate at 20 µg
Secondary
IR Dye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/15000 dilution
Performed under reducing conditions.
Predicted band size : 57 kDa
Observed band size : 57 kDa
Several smaller bands are seen in Human Liver Whole Tissue Lysate. These are predicted to be break-down products of PDI; the banding pattern is consistent with that observed in Liver lysates for other available PDI antibodies.

Image courtesy of Human Protein Atlas
ab31811 staining PDI in Human gall bladder. The paraffin embedded tissue was incubated with ab31811 (1/800 dilution) for 30 mins at room temperature. Antigen retrieval was performed by heat induction in citrate buffer pH 6. ab31811 was tested in a tissue microarray (TMA) containing a wide range of normal and cancer tissues as well as a cell microarray consisting of a range of commonly used, well characterised human cell lines.
Further results for this antibody can be found at www.proteinatlas.org

ICC/IF image of ab31811 stained human HEK 293 cells. The cells were 4% PFA fixed (10 min), permabilised in 0.1% PBS-Tween (20 min) and incubated with the antibody (ab31811, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue). This antibody also gave a positive IF result in HeLa and MCF7 cells.

All lanes : Anti-PDI antibody - ER Marker (ab31811) at 1 µg/ml
Lane 1 : Liver (Mouse) Tissue Lysate
Lane 2 : Liver (Rat) Tissue Lysate
Lysates/proteins at 10 µg per lane.
Secondary
Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP), pre-adsorbed (ab97080) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 57 kDa
Observed band size : 57 kDa
Exposure time : 30 seconds

IHC image of ab31811 staining in pancreas formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab31811, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
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