Anti-VAMP4 抗体 [EPR25066-77] (ab290726)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR25066-77] to VAMP4
- Suitable for: ICC/IF, IHC-P, Flow Cyt (Intra), IHC-Fr, WB, IP
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
製品の概要
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製品名
Anti-VAMP4 antibody [EPR25066-77]
VAMP4 一次抗体 製品一覧 -
製品の詳細
Rabbit monoclonal [EPR25066-77] to VAMP4 -
由来種
Rabbit -
特異性
Please note this antibody does not react with Human species for ICC application.
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アプリケーション
適用あり: ICC/IF, IHC-P, Flow Cyt (Intra), IHC-Fr, WB, IPmore details -
種交差性
交差種: Mouse, Rat, Human -
免疫原
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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ポジティブ・コントロール
- WB: SH-SY5Y, Jurkat, K-562, 293T, HeLa, C6, RAW264.7, PC-12, NIH/3T3 whole cell lysates. Human testis, Mouse brain, Mouse testis, Rat brain, Rat testis whole tissue lysates. IHC-P: human cerebrum, mouse cerebrum, mouse testis, rat cerebrum, rat testis tissues. ICC/IF: RAW 264.7. IHC-Fr: mouse testis, rat testis. Flow cyt (Intra): RAW 264.7, 293T. IP: 293T, RAW264.7
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特記事項
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
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製品の状態
Liquid -
保存方法
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. -
バッファー
pH: 7.2
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA -
Concentration information loading...
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精製度
Protein A purified -
ポリ/モノ
モノクローナル -
クローン名
EPR25066-77 -
アイソタイプ
IgG -
研究分野
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ab290726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 |
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ICC/IF |
1/50.
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IHC-P |
1/500.
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Flow Cyt (Intra) |
1/50.
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IHC-Fr |
1/500.
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WB |
1/1000. Predicted molecular weight: 16 kDa.
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IP |
1/30.
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特記事項 |
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ICC/IF
1/50. |
IHC-P
1/500. |
Flow Cyt (Intra)
1/50. |
IHC-Fr
1/500. |
WB
1/1000. Predicted molecular weight: 16 kDa. |
IP
1/30. |
ターゲット情報
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機能
Involved in the pathway that functions to remove an inhibitor (probably synaptotagmin-4) of calcium-triggered exocytosis during the maturation of secretory granules. May be a marker for this sorting pathway that is critical for remodeling the secretory response of granule. -
配列類似性
Belongs to the synaptobrevin family.
Contains 1 v-SNARE coiled-coil homology domain. -
細胞内局在
Golgi apparatus > trans-Golgi network membrane. Associated with trans Golgi network (TGN) and newly formed immature secretory granules (ISG). Not found on the mature secretory organelles. - Information by UniProt
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参照データベース
- Entrez Gene: 8674 Human
- Entrez Gene: 53330 Mouse
- Entrez Gene: 364033 Rat
- Omim: 606909 Human
- SwissProt: A2IDD8 Human
- SwissProt: O75379 Human
- SwissProt: O70480 Mouse
- Unigene: 6651 Human
see all -
別名
- VAMP 24 antibody
- VAMP 4 antibody
- VAMP-4 antibody
see all
画像
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All lanes : Anti-VAMP4 antibody [EPR25066-77] (ab290726) at 1/1000 dilution
Lane 1 : SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate.
Lane 2 : Human testis tissue lysate.
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 16 kDa
Observed band size: 18 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesBlocking / Dilution buffer and concentration: 5% NFDM/TBST
The expression profile/molecular weight observed is consistent with that described in the literature (PMID: 10359608).
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All lanes : Anti-VAMP4 antibody [EPR25066-77] (ab290726) at 1/1000 dilution
Lane 1 : Jurkat (human T cell leukemia T lymphocyte) whole cell lysate.
Lane 2 : K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate
Lane 3 : 293T (human embryonic kidney epithelial cell) whole cell lysate.
Lane 4 : HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate.
Lysates/proteins at 40 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 16 kDa
Observed band size: 18 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesBlocking / Dilution buffer and concentration: 5% NFDM/TBST
The expression profile/molecular weight observed is consistent with that described in the literature (PMID: 10359608).
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All lanes : Anti-VAMP4 antibody [EPR25066-77] (ab290726) at 1/1000 dilution
Lane 1 : Mouse brain tissue lysate.
Lane 2 : Mouse testis tissue lysate.
Lane 3 : Mouse skeletal muscle tissue lysate.
Lane 4 : Rat brain tissue lysate.
Lane 5 : Rat testis tissue lysate.
Lane 6 : Rat skeletal muscle tissue lysate.
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 16 kDa
Observed band size: 18 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesBlocking / Dilution buffer and concentration: 5% NFDM/TBST
The expression profile/molecular weight observed is consistent with that described in the literature (PMID: 10359608).
Negative control: skeletal muscle (PMID: 10359608) -
All lanes : Anti-VAMP4 antibody [EPR25066-77] (ab290726) at 1/1000 dilution
Lane 1 : C6 (rat glial tumor glial cell) whole cell lysate.
Lane 2 : RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate.
Lane 3 : PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate.
Lane 4 : 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 1/100000 dilution
Predicted band size: 16 kDa
Observed band size: 18 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesBlocking / Dilution buffer and concentration: 5% NFDM/TBST
The expression profile/molecular weight observed is consistent with that described in the literature (PMID: 10359608).
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Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labelling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) followed by a ready to use LeicaDS9800 (BONDTM Polymer Refine Detection). Cytoplasmic staining on human cerebrum.The section was incubated with ab290726 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 LeicaDS9800 (BONDTM Polymer Refine Detection) was used.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
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Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) followed by a ready to use LeicaDS9800 (BONDTM Polymer Refine Detection). Cytoplasmic staining on mouse cerebrum (PMID: 16506193). The section was incubated with ab290726 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 LeicaDS9800 (BONDTM Polymer Refine Detection) was used.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
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Immunohistochemical analysis of paraffin-embedded Mouse testis tissue labelling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) followed by a ready to use LeicaDS9800 (BONDTM Polymer Refine Detection). Cytoplasmic staining on mouse testis. The section was incubated with ab290726 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 LeicaDS9800 (BONDTM Polymer Refine Detection) was used.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
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Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labelling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) followed by a ready to use LeicaDS9800 (BONDTM Polymer Refine Detection) was used. Cytoplasmic staining on rat cerebrum. The section was incubated with ab290726 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 LeicaDS9800 (BONDTM Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
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Immunohistochemical analysis of paraffin-embedded Rat testis tissue labelling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) followed by a ready to use LeicaDS9800 (BONDTM Polymer Refine Detection). Cytoplasmic staining on rat testis. The section was incubated with ab290726 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 LeicaDS9800 (BONDTM Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
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Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse testis (fresh) tissue labeling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 µg/mL) dilution (Green). Positive staining on mouse testis is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 µg/mL) dilution.
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Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse skeletal muscle (fresh) tissue labeling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 µg/mL) dilution (Green). Negative control (PMID:10359608) No staining on mouse skeletal muscle is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 µg/mL) dilution.
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Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat testis (fresh) tissue labeling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 µg/mL) dilution (Green). Positive staining on rat testis is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 µg/mL) dilution.
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Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat skeletal muscle (fresh) tissue labeling VAMP4 with ab290726 at 1/500 (1.102 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 µg/mL) dilution (Green). Negative control (PMID:10359608). No staining on rat skeletal muscle is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 (2 µg/mL) dilution.
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Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeilized RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) cells lebelling VAMP4 with ab290726 at 1/50 (11.02 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 in RAW 264.7 cell line is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (2.5 ug/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.
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Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized 293T (Human embryonic kidney epithelial cell) cells labelling VAMP4 with ab290726 at 1/50 dilution (1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
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Intracellular flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized RAW 264.7 (Mouse Abelson murine leukemia virus-induced tumor macrophage) cells labelling VAMP4 with ab290726 at 1/50 dilution (1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
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VAMP4 was immunoprecipitated from 0.35 mg 293T (human embryonic kidney epithelial cell) whole cell lysate 10 ug with ab290726 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab290726 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1: 293T (human embryonic kidney epithelial cell) whole cell lysate 10 ug
Lane 2: ab290726 IP in 293T whole cell lysate
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab290726 in 293T whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 93 seconds
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VAMP4 was immunoprecipitated from 0.35 mg RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate 10 ug with ab290726 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab290726 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1: RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate 10 ug
Lane 2: ab290726 IP in RAW264.7 whole cell lysate
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab290726 in RAW264.7 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 93 seconds
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
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SDS download
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Datasheet download
Certificate of Compliance
参考文献 (0)
ab290726 は論文での使用が確認できていません。