Anti-XBP1 antibody [EPR22004] - BSA and Azide free (ab238456)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR22004] to XBP1 - BSA and Azide free
- Suitable for: WB, Flow Cyt, IP
- Reacts with: Mouse, Human
Overview
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Product name
Anti-XBP1 antibody [EPR22004] - BSA and Azide free
See all XBP1 primary antibodies -
Description
Rabbit monoclonal [EPR22004] to XBP1 - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: WB, Flow Cyt, IPmore details -
Species reactivity
Reacts with: Mouse, Human -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- Flow Cyt: Huh7 treated with 300 nM Thapsigargin for 18 hours.
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General notes
Ab238456 is the carrier-free version of ab220783. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
ab238456 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR22004 -
Isotype
IgG -
Research areas
Images
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XBP1 was immunoprecipitated from 0.35 mg Huh7 (human hepatocellular carcinoma epithelial cell line) treated with 300 nM Thapsigargin for 18 hours whole cell lysate with ab220783 at 1/50 dilution. Western blot was performed from the immunoprecipitate using ab220783 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/5000 dilution.
Lane 1: Huh7 treated with 300 nM Thapsigargin for 18 hours whole cell lysate 10 µg (Input).
Lane 2: ab220783 IP in Huh7 treated with 300 nM Thapsigargin for 18 hours whole cell lysate (+).
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab220783 in Huh7 treated with 300 nM Thapsigargin for 18 hours whole cell lysate (-).Blocking/Dilution buffer: 5% NFDM/TBST.
Exposure time: 3 minutes.This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab220783).
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Flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized Huh7 (human hepatocellular carcinoma epithelial cell line) cells treated with 300 nM Thapsigargin for 18 hours (red) / Untreated control (green) labeling XBP1 with ab220783 at 1/100 dilution compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells incubated with secondary antibody only) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and sodium azide (ab220783).
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