Anti-SLC26A2/DTD antibody - N-terminal (ab191158)
Key features and details
- Rabbit polyclonal to SLC26A2/DTD - N-terminal
- Suitable for: WB, IP
- Reacts with: Human
- Isotype: IgG
Overview
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Product name
Anti-SLC26A2/DTD antibody - N-terminal
See all SLC26A2/DTD primary antibodies -
Description
Rabbit polyclonal to SLC26A2/DTD - N-terminal -
Host species
Rabbit -
Tested Applications & Species
See all applications and species dataApplication Species IP HumanWB Human
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Immunogen
Synthetic peptide within Human SLC26A2/DTD aa 1-100 (N terminal). The exact immunogen sequence used to generate this antibody is proprietary information. If additional detail on the immunogen is needed to determine the suitability of the antibody for your needs, please contact our Scientific Support team to discuss your requirements. (NP_000103.2).
Database link: P50443 -
Positive control
- HeLa and 293T whole cell lysates.
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General notes
This product was previously labelled as SLC26A2
Properties
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Form
Liquid -
Storage instructions
Shipped 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 buffer
pH: 7
Preservative: 0.09% Sodium azide
Constituent: 99% Tris citrate/phosphate
pH 7 to 8 -
Concentration information loading... -
Purity
Immunogen affinity purified -
Purification notes
ab191158 was affinity purified using an epitope specific to SLC26A2/DTD immobilized on solid support. -
Clonality
Polyclonal -
Isotype
IgG -
Research areas
Images
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Western blot - Anti-SLC26A2/DTD antibody - N-terminal (ab191158)All lanes : Anti-SLC26A2/DTD antibody - N-terminal (ab191158) at 0.1 µg/ml
Lane 1 : HeLa whole cell lysate
Lane 2 : 293T whole cell lysate
Lane 3 : Jurkat whole cell lysate
Lysates/proteins at 50 µg per lane.
Developed using the ECL technique.
Predicted band size: 82 kDa
Exposure time: 3 minutesLysates prepared using RIPA lysis buffer.
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Immunoprecipitation - Anti-SLC26A2/DTD antibody - N-terminal (ab191158)Detection of SLC26A2/DTD in Immunoprecipitates of HeLa whole cell lysate prepared using RIPA lysis buffer (1 mg for IP, 20% of IP loaded), using ab191158 at 6 µg/mg lysate for IP and at 1 µg/ml for subsequent Western blot detection.
Detection: Chemiluminescence with an exposure time of 3 minutes.
