HA-Tag 抗体
(1 reference)
(2 validations)Our Local Distributor
北京 101111
Quick Overview for HA-Tag 抗体 (ABIN2443910)
抗原
适用
宿主
克隆类型
标记
应用范围
克隆位点
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序列
- YPYDVPDYA
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纯化方法
- Purified
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亚型
- IgG3
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anti-HA-Tag antibody
WB, ELISA, IP, IF, FACS 宿主: 小鼠 Monoclonal 18B11H6 unconjugated
anti-HA-Tag antibodyWB, IF, ChIP 宿主: 兔 Polyclonal RB0411 unconjugated
anti-HA-Tag antibodyWB, ELISA, IP 宿主: 兔 Polyclonal unconjugated
anti-HA-Tag antibodyWB, ELISA, IF, ChIP 宿主: 兔 Polyclonal unconjugated
anti-HA-Tag (AA 98-106) antibodyAnimal-Free 适用: 标记 WB, ELISA, IF 宿主: 兔 Monoclonal AB158-1-D11 unconjugated Recombinant Antibody
anti-HA-Tag antibody (HRP)WB, ELISA, IP 宿主: 小鼠 Monoclonal 5E11D8 HRP
anti-HA-Tag antibody适用: 标记 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-HA-Tag (AA 98-106) antibodyAnimal-Free 适用: 标记 WB, ELISA, IF 宿主: 小鼠 Monoclonal AB158-1-D11 unconjugated Recombinant Antibody
anti-HA-Tag antibodyELISA, Coat 宿主: 小鼠 Monoclonal 16-43 unconjugated
anti-HA-Tag antibodyWB, IP, IF, IC 宿主: 小鼠 Monoclonal unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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- by
- Georg-August-University of Göttingen, Johann-Friedrich-Blumenbach-Institute for Zoology and Anthropology, Developmental Biology
- No.
- #100058
- 日期
- 2016.09.16
- 抗原
- HA-Tag
- Lot Number
- 16631508212-P
- Method validated
- Western Blotting
- Positive Control
- HA-fusion proteins expressed in NIH/3T3 cells
- Negative Control
- Notes
- Passed, regarding sensitivity and specificity. The HA-tag antibody ABIN2443910 does specifically recognize HA-tagged proteins in whole cell lysates from human tissue culture cells with no obvious background staining.
- Primary Antibody
- ABIN2443910
- Secondary Antibody
- Rabbit anti-Mouse IgG (whole molecule), HRP-linked (Sigma-Aldrich, A9044, lot number: 034M4761)
- Full Protocol
- Cultured NIH/3T3 cells heterologously expressing either a 26kDa (Fig. A) or 43kDa (Fig. B) HA-tag-fusion protein were rinsed with PBS and lysed in 6M Urea/20mM Tris.
- 40µg total protein were used for Western blot analysis.
- Proteins were denatured and separated on 10% SDS-PAGE (Laemmli 1970) and blotted to Amersham Protran Premium 0.2 NC (GE Healthcare, 10600004, lot A10043108) (Towbin et al., 1979).
- Blocking of membrane in 5% skim milk in TBST (50 mM Tris-HCl, pH 7.4, 150mM NaCl, 0.1% Tween 20) for 30min at RT.
- Incubation with primary antibody ABIN2443910 diluted 1:600 in 5% skim milk in TBST overnight at 4°C.
- Washing in TBST for 30min at RT.
- Incubation with secondary antibody secondary antibody: rabbit-anti-mouse IgG (whole molecule), HRP-linked (Sigma-Aldrich, A9044, lot 034M4761) diluted 1:10000 in 5% skim milk in TBST for 45min at RT.
- Washing in TBST for 30-45min at RT.
- Chemiluminescence detection using Clarity Western ECL Substrate (BioRad, 170-5061) according to the supplier’s recommendations and image capture via X-ray films.
- Experimental Notes
- A dilution factor <1000 is recommended for Western blot on cellular lysates with ABIN2443910.
生效 #100058 (Western Blotting)!['独立验证'标志]( "成功验证")
!['独立验证'标志]( "成功验证")
Validation Images![HA-tagged fusion proteins were expressed in NIH/3T3 cells. Whole cell lysates were separated by SDS-PAGE and the tagged protein detected using anti HA-tag antibody ABIN2443910 diluted 1:600. Expected molecular mass of the fusion proteins were approximately 26kDa (A.) and 43kDa (B.) respectively. The left lane corresponds in both blots A. and B. to the pellet, the right to the supernatant after centrifugation. Exposition time for image capture on X-ray films: 1min (A.) and 30min (B.). For C., samples were prepared as for B. but the anti HA-tag antibody ABIN2443910 was diluted 1:1000. Exposure time: 15min.]()
HA-tagged fusion proteins were expressed in NIH/3T3 cells. Whole cell lysates were separated by SDS-PAGE and the tagged protein detected using anti HA-tag antibody ABIN2443910 diluted 1:600. Expected molecular mass of the fusion proteins were approximately 26kDa (A.) and 43kDa (B.) respectively. The left lane corresponds in both blots A. and B. to the pellet, the right to the supernatant after centrifugation. Exposition time for image capture on X-ray films: 1min (A.) and 30min (B.). For C., samples were prepared as for B. but the anti HA-tag antibody ABIN2443910 was diluted 1:1000. Exposure time: 15min.
Full Methods -
- by
- Georg-August-University of Göttingen, Johann-Friedrich-Blumenbach-Institute for Zoology and Anthropology, Developmental Biology
- No.
- #100059
- 日期
- 2016.09.16
- 抗原
- HA-Tag
- Lot Number
- 16631508212-P
- Method validated
- Immunocytochemistry
- Positive Control
- HA-fusion proteins transiently expressed in NIH/3T3 cells
- Negative Control
- Notes
- Passed, regarding sensitivity and specificity. The antibody specifically detects the HA-fusion protein in immuno-cytochemical experiments. No obvious background staining was found.
- Primary Antibody
- ABIN2443910
- Secondary Antibody
- MFP488 goat anti-mouse IgG (H+L) (MoBiTec, MFP-A1029, lot 2803101)
- Full Protocol
- NIH/3T3 cells (ATCC) were grown on cover slips in DMEM, 10% fetal bovine serum, 5% penicillin/streptomycin (all Gibco) at 37°C in 5% CO2.
- Cells were transfected using Metafectene Pro (Biontex, T040-1.0, lot AD1.13) according to the manual with a plasmid encoding an HA-tag fusion protein that is expected to localize to the nuclear membrane and the cytoplasm.
- 24h post-transfection cells were fixed in 3.7% paraformaldehyde in PBS for 15min and processed for immuno-cytology.
- Unspecific binding sites were blocked in PBST (phosphate buffered saline containing 0.15% bovine serum albumin, 0.1% Tween-20) for 1h.
- Cells were incubated with the primary antibody ABIN2443910 diluted 1:100 in PBS at 4°C overnight.
- Cells were washed in TBST (50mM Tris-HCl, pH 7.4, 150mM NaCl, 0.1% Tween 20) for 15min.
- Incubation with the secondary antibody MFP488 goat anti-mouse IgG (H+L) (MoBiTec, MFP-A1029, lot 2803101) diluted 1:600 in PBS and DAPI (stock solution 10µg/µl, diluted 1:500) for 1h at 37°C.
- Cells were washed in TBST for 15min.
- Cells were embedded in Fluorescent Mounting Medium (Dako, S3023, lot 10090890).
- Images were taken by confocal microscopy (LSM 510, Zeiss), and processed using Adobe Photoshop 5.0.
- Experimental Notes
- none
生效 #100059 (Immunocytochemistry)!['独立验证'标志]( "成功验证")
!['独立验证'标志]( "成功验证")
Validation Images![HA-tagged fusion proteins were expressed in NIH/3T3 cells. The protein of interest is expected to localize to the nuclear membrane and the cytoplasm. A. The fusion protein was revealed via its HA-tag at the nuclear membrane and in the cytoplasm using ABIN2443910 (green; DAPI counterstain in blue). B. Co-staining of the fusion protein with using using anti-HA tag antibody ABIN2443910 (green) and an anti-myc-tag antibody (red; unspecific background staining caused by the transfection reagent). DAPI staining was used to visualize the nucleus (blue).]()
HA-tagged fusion proteins were expressed in NIH/3T3 cells. The protein of interest is expected to localize to the nuclear membrane and the cytoplasm. A. The fusion protein was revealed via its HA-tag at the nuclear membrane and in the cytoplasm using ABIN2443910 (green; DAPI counterstain in blue). B. Co-staining of the fusion protein with using using anti-HA tag antibody ABIN2443910 (green) and an anti-myc-tag antibody (red; unspecific background staining caused by the transfection reagent). DAPI staining was used to visualize the nucleus (blue).
Full Methods -
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储存条件
- 4 °C/-20 °C/-80 °C
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储存方法
- Lyophilized antibodies can be kept at 4ºC for up to 3 months and should be kept at -20ºC for long-term storage (2 years). To avoid freeze-thaw cycles, reconstituted antibodies should be aliquoted before freezing for long-term (1 year) storage (-80ºC) or kept at 4ºC for short-term usage (2 months).
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: "APOBEC3-mediated restriction of RNA virus replication." in: Scientific reports, Vol. 8, Issue 1, pp. 5960, (2019) (PubMed).
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: "APOBEC3-mediated restriction of RNA virus replication." in: Scientific reports, Vol. 8, Issue 1, pp. 5960, (2019) (PubMed).
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- HA-Tag
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别名
- HA Tag
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物质类
- Tag
抗原
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