Anti-F4/80 抗体 [EPR26545-166] (BSA and Azide free) (ab300422)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR26545-166] to F4/80 - BSA and Azide free
- Suitable for: IHC-Fr, IHC-P, WB, mIHC, ICC/IF
- Reacts with: Mouse, Rat
Related conjugates and formulations
製品の概要
-
製品名
Anti-F4/80 antibody [EPR26545-166] (BSA and Azide free)
F4/80 一次抗体 製品一覧 -
製品の詳細
Rabbit monoclonal [EPR26545-166] to F4/80 - BSA and Azide free -
由来種
Rabbit -
アプリケーション
適用あり: IHC-Fr, IHC-P, WB, mIHC, ICC/IFmore details
適用なし: Flow Cyt -
種交差性
交差種: Mouse, Rat -
免疫原
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
-
ポジティブ・コントロール
- WB: J774A.1 (mouse reticulum cell sarcoma macrophage), RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage), Mouse spleen tissue. IHC: Mouse liver, mouse spleen, rat liver, rat spleen. IHC/FR: Mouse spleen (fresh). ICC/IF: RAW 264.7. mIHC: Mouse spleen, mouse bone marrow, mouse thymus, mouse lymph node
-
特記事項
ab300422 is a carrier free version of ab300421.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
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.
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.
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.
製品の特性
-
製品の状態
Liquid -
保存方法
Shipped at 4°C. Store at +4°C. -
バッファー
pH: 7.2
Constituent: 100% PBS -
キャリア・フリー
はい -
Concentration information loading...
-
精製度
Protein A purified -
ポリ/モノ
モノクローナル -
クローン名
EPR26545-166 -
アイソタイプ
IgG -
研究分野
関連製品
-
Alternative Versions
-
Compatible Secondaries
アプリケーション
The Abpromise guarantee
Abpromise保証は、 次のテスト済みアプリケーションにおけるab300422の使用に適用されます
アプリケーションノートには、推奨の開始希釈率がありますが、適切な希釈率につきましてはご検討ください。
アプリケーション | Abreviews | 特記事項 |
---|---|---|
IHC-Fr |
Use at an assay dependent concentration.
|
|
IHC-P |
Use at an assay dependent concentration.
|
|
WB |
Use at an assay dependent concentration. Predicted molecular weight: 97 kDa.
|
|
mIHC |
Use at an assay dependent concentration.
|
|
ICC/IF |
Use at an assay dependent concentration.
|
特記事項 |
---|
IHC-Fr
Use at an assay dependent concentration. |
IHC-P
Use at an assay dependent concentration. |
WB
Use at an assay dependent concentration. Predicted molecular weight: 97 kDa. |
mIHC
Use at an assay dependent concentration. |
ICC/IF
Use at an assay dependent concentration. |
ターゲット情報
-
機能
Orphan receptor involved in cell adhesion and probably in cell-cell interactions specifically involving cells of the immune system. May play a role in regulatory T-cells (Treg) development. -
組織特異性
Expression is restricted to eosinophils. -
配列類似性
Belongs to the G-protein coupled receptor 2 family. Adhesion G-protein coupled receptor (ADGR) subfamily.
Contains 6 EGF-like domains.
Contains 1 GPS domain. -
細胞内局在
Cell membrane. - Information by UniProt
-
参照データベース
- Entrez Gene: 13733 Mouse
- Entrez Gene: 316137 Rat
- SwissProt: Q61549 Mouse
- SwissProt: Q5Y4N8 Rat
- Unigene: 2254 Mouse
-
別名
- ADGRE1 antibody
- Adhesion G protein coupled receptor E1 antibody
- Adhesion G protein-coupled receptor E1 antibody
see all
画像
-
All lanes : Anti-F4/80 antibody [EPR26545-166] (ab300421) at 1/1000 dilution
Lane 1 : J774A.1 (mouse reticulum cell sarcoma macrophage) whole cell lysate
Lane 2 : NIH/3T3 (mouse embryonic fibroblast) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 97 kDa
Observed band size: 90-160 kDa why is the actual band size different from the predicted?
Exposure time: 15 secondsThis data was developed using ab300421, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Negative control: NIH/3T3 (PMID:8550607).
The antibody recognizes glycosylated form (120~160KDa) and unglycosylated form(~90KDa) of F4/80(PMID:10547361) in the unboiled samples.
-
All lanes : Anti-F4/80 antibody [EPR26545-166] (ab300421) at 1/1000 dilution
Lane 1 : RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) whole cell lysate
Lane 2 : L-929 ( mouse connective tissue fibroblast) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 97 kDa
Observed band size: 160 kDa why is the actual band size different from the predicted?
Exposure time: 15 secondsThis data was developed using ab300421, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Negative control: L-929 (PMID:8550607).
The samples are unboiled.
-
Anti-F4/80 antibody [EPR26545-166] (ab300421) at 1/1000 dilution + Mouse spleen tissue lysate 20 µg
Secondary
Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 97 kDa
Exposure time: 26 secondsThis data was developed using ab300421, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The samples are unboiled.
-
This data was developed using ab300421, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections of mouse liver tissue labelling F4/80 with ab300421 at 1/5000 dilution for 30min at room temperature, followed by LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on the Kupffer cells of Mouse liver (PMID: 26473015) is observed. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control: The secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution) for 20 mins.
-
This data was developed using ab300421, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections of mouse spleen tissue labelling F4/80 with ab300421 at 1/5000 dilution for 30min at room temperature, followed by LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on the macrophages of mouse spleen (PMID: 19820169) is observed. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control: The secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution) for 20 mins.
-
This data was developed using ab300421, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections of rat liver tissue labelling F4/80 with ab300421 at 1/5000 dilution for 30min at room temperature, followed by LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on the Kupffer cells of rat liver is observed. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control: The secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution) for 20 mins.
-
This data was developed using ab300421, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of Paraffin-embedded sections of Rat spleen tissue labelling F4/80 with ab300421 at 1/5000 dilution for 30min at room temperature, followed by LeicaDS9800 (Bond™ Polymer Refine Detection). Positive staining on the macrophages of rat spleen is observed. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
Counterstained with Hematoxylin.
Secondary antibody only control: The secondary antibody is LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution) for 20 mins.
-
This data was developed using ab300421, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 0.2% Triton X-100 permeabilised, 4% PFA fixed of fresh Mouse spleen tissue labelling F4/80 with ab300421 at 1/500 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081) at 1/1000 dilution. Positive staining on the macrophages of mouse spleen is observed.
The nuclear countertain is DAPI.
-
This data was developed using ab300421, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde fixed, 0.1% TritonX-100 permeabilised RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) labelling F4/80 with ab300421 at 1/50 dilution, followed Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081) secondary antibody at 1/1000 dilution. Confocal image showing membranous and cytoplasmic staining in RAW264.7 cell line. Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594)(ab195889) was used to counterstain Microtubule at 1/200 dilution. The nuclear counterstain is DAPI.
Negative control: NIH/3T3 (PMID: 8550607).
プロトコール
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
データシートおよび資料
-
Datasheet download
Certificate of Compliance
参考文献 (3)
ab300422 は 3 報の論文で使用されています。
- Hichami A et al. In Vitro Functional Characterization of Type-I Taste Bud Cells as Monocytes/Macrophages-like Which Secrete Proinflammatory Cytokines. Int J Mol Sci 24:N/A (2023). PubMed: 37373472
- Dai Y et al. A construct of adipose-derived mesenchymal stem cells-laden collagen scaffold for fertility restoration by inhibiting fibrosis in a rat model of endometrial injury. Regen Biomater 10:rbad080 (2023). PubMed: 37808957
- Ding Z et al. Nanosized Silk-Magnesium Complexes for Tissue Regeneration. Adv Healthc Mater 12:e2300887 (2023). PubMed: 37317936