Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal TREM2 antibody. Carrier free. Suitable for ICC/IF, WB, IHC-P and reacts with Mouse, Transfected cell line - Mouse samples.
View Alternative Names
Trem2a, Trem2b, Trem2c, Trem2, Triggering receptor expressed on myeloid cells 2, TREM-2, Triggering receptor expressed on monocytes 2
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free (AB305072)
This data was developed using ab305103, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) cell pellet and (B) Neuro-2a (mouse neuroblastoma neuroblast) cell pellet, labeling TREM2 with ab305103 at 1/500 dilution (1.014 µg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit.
The section was incubated with ab305103 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin.
Positive staining in RAW264.7 cell pellet was observed with no staining in Neuro-2a cell pellet. Secondary antibody only control : RAW264.7 cell pellet with only ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free (AB305072)
This data was developed using ab305103, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded tissue labeling Trem2 with ab305103 at 1/500 dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) whole brain tissue up to postnatal day 5 (P5) from wild-type C57BL/6JGpt mice and no staining on (B) whole brain tissue up to postnatal day 5 (P5) from TREM2 knockout mice
The section was incubated with ab305103 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Trem2-KO homozygous mice (Strain ID : T003346).
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free (AB305072)
Immunohistochemical analysis of paraffin-embedded (A) HEK-293T cells transfected with a mouse TREM2 expression vector containing a GFP tag and (B) HEK-293T cells transfected with an empty vector containing a GFP tag (labeling TREM2 with ab305103 at 1/500 (1.014 µg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) was used. Positive staining on (A) HEK-293T cells transfected with a Trem2 expression vector containing a GFP tag. No staining on (B) HEK-293T cells transfected with empty vector containing a GFP tag. The section was incubated with ab305103 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins. This data was developed using ab305103, the same antibody clone in a different buffer formulation.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free (AB305072)
This data was developed using ab305103, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) cells labelling TREM2 with ab305103 at 1/500 (1.014 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/mL dilution (Green). Confocal image showing cytoplasmic staining on RAW 264.7 cell line.Negative control : Neuro-2a (PMID : 19302484).Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free (AB305072)
Immunohistochemical analysis of paraffin-embedded (A) FAD4T Transgenic mouse Alzheimer’s disease cerebrum and (B) Mouse normal cerebrum (labeling TREM2 with ab305103 at 1/500 (1.014 µg/ml) followed by a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) was used. Positive staining on (A) Mouse Alzheimer’s disease cerebrum, no staining on (B) Mouse normal cerebrum. The section was incubated with ab305103 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use Leica DS9800 (Bond™ Polymer Refine Detection) kit. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins. This data was developed using ab305103, the same antibody clone in a different buffer formulation.
- WB
Supplier Data
Western blot - Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free (AB305072)
This data was developed using ab305103, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST TREM2 is a glycoprotein of approximately 35-50 kDa and detected as a 25 kDa band after treated with Protein Deglycosylation MIX II. The identity of the higher MW band at approximately 70 kDa is unknown.
All lanes:
Western blot - Anti-TREM2 antibody [EPR26210-1] (<a href='/en-us/products/primary-antibodies/trem2-antibody-epr26210-1-ab305103'>ab305103</a>) at 1/1000 dilution
Lane 1:
Untreated J774A.1 (mouse reticum cell sarcoma monocyte macrophage), whole cell lysate at 30 µg
Lane 2:
J774A.1 whole cell lysate treated with Protein Deglycosylation Mix II at 30 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 35-50 kDa,25 kDa
Observed band size: 35-50 kDa,25 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-TREM2 antibody [EPR26210-1] - BSA and Azide free (AB305072)
This data was developed using ab305103, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST The expression profile and molecular weight observed are consistent with what has been described in the literature (PMID : 29611543; PMID : 28559417). Negative control : L929, F9 (PMID : 11241283), Neuro-2a (PMID : 19302484). The identity of the higher MW band at approximately 70 kDa is unknown.
All lanes:
Western blot - Anti-TREM2 antibody [EPR26210-1] (<a href='/en-us/products/primary-antibodies/trem2-antibody-epr26210-1-ab305103'>ab305103</a>) at 1/1000 dilution
Lane 1:
J774A.1 (mouse reticum cell sarcoma monocyte macrophage), whole cell lysate at 20 µg
Lane 2:
RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), whole cell lysate at 20 µg
Lane 3:
N9 (mouse microglia), whole cell lysate at 20 µg
Lane 4:
L929 (mouse connective tissue fibroblast), whole cell lysate at 20 µg
Lane 5:
Neuro-2a (mouse neuroblastoma neuroblast), whole cell lysate at 20 µg
Lane 6:
F9 (mouse embryonal carcinoma epithelial cell), whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 25 kDa
Observed band size: 35-50 kDa
false
Exposure time: 3min
Related conjugates and formulations (8)
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Anti-TREM2 antibody [EPR26210-1]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-TREM2 antibody [EPR26210-1]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-TREM2 antibody [EPR26210-1]
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578 PE
PE Anti-TREM2 antibody [EPR26210-1]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-TREM2 antibody [EPR26210-1]
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660 APC
APC Anti-TREM2 antibody [EPR26210-1]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-TREM2 antibody [EPR26210-1]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-TREM2 antibody [EPR26210-1]
Reactivity data
Product details
What are the advantages of a recombinant monoclonal antibody?
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 batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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