Anti-TG6 antibody [EPR10308] - BSA and Azide free (ab250287)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR10308] to TG6 - BSA and Azide free
- Suitable for: ICC, IHC-P, Flow Cyt, WB
- Reacts with: Mouse, Rat, Human
Overview
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Product name
Anti-TG6 antibody [EPR10308] - BSA and Azide free
See all TG6 primary antibodies -
Description
Rabbit monoclonal [EPR10308] to TG6 - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: ICC, IHC-P, Flow Cyt, WBmore details -
Species reactivity
Reacts with: Mouse, Rat, Human -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- ICC: Raw 264.7 and MOLT-4 cells. WB: MOLT-4, CTLL-2, EL4, RAW 264.7 and NIH/3T3 cell lysates; Human kidney lysate; Mouse kidney lysate.
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General notes
Ab250287 is the carrier-free version of ab180959. 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
ab250287 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
Affinity purified -
Clonality
Monoclonal -
Clone number
EPR10308 -
Isotype
IgG -
Research areas
Images
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Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Raw 264.7 cells labelling TG6 with ab180959 at 1/50 dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (2 µg/mL) (Green). Confocal image showing membranous staining in RAW 264.7 cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 µg/mL) (Red). The nuclear counterstain was DAPI (Blue).
Secondary antibody only control: PBS instead of the primary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab180959).
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All lanes : Anti-TG6 antibody [EPR10308] - N-terminal (ab180959) at 1/1000 dilution
Lane 1 : MOLT-4 (Human lymphoblastic leukemia T lymphoblast) cell lysate
Lane 2 : Human kidney lysate
Lane 3 : Mouse kidney lysate
Lane 4 : CTLL-2 (Mouse T lymphocyte) cell lysate
Lane 5 : EL4 (Mouse lymphoma T lymphocyte) cell lysate
Lane 6 : RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cell lysate
Lane 7 : NIH/3T3 (Mouse embryonic fibroblast) cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 79 kDa
Observed band size: 75 kDa why is the actual band size different from the predicted?Blocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time: 70 s
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Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized MOLT-4 cells labelling TG6 with ab180959 at 1/50 dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (2 µg/mL) (Green). Confocal image showing membranous staining in MOLT-4 cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 µg/mL) (Red). The nuclear counterstain was DAPI (Blue).
Secondary antibody only control: PBS instead of the primary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab180959).
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