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Anti-14-3-3 zeta/delta Antibody (7T9)

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产品编号 TMAH-01260

Anti-14-3-3 zeta/delta Antibody (7T9) 是一种 Mouse 抗体,靶向 14-3-3 zeta/delta。Anti-14-3-3 zeta/delta Antibody (7T9) 可用于 ELISA, WB, IHC, IF, FC。

Anti-14-3-3 zeta/delta Antibody (7T9)

Anti-14-3-3 zeta/delta Antibody (7T9)

Rating icon 还可以
产品编号 TMAH-01260

Anti-14-3-3 zeta/delta Antibody (7T9) 是一种 Mouse 抗体,靶向 14-3-3 zeta/delta。Anti-14-3-3 zeta/delta Antibody (7T9) 可用于 ELISA, WB, IHC, IF, FC。

规格价格库存数量
50 μL
¥ 1,310
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100 μL
¥ 2,185
5日内发货
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产品介绍

生物活性
产品描述
Anti-14-3-3 zeta/delta Antibody (7T9) is a Mouse antibody targeting 14-3-3 zeta/delta. Anti-14-3-3 zeta/delta Antibody (7T9) can be used in ELISA, WB, IHC, IF, FC.
Ig Type
IgG2b
克隆号
7T9
交叉反应
Human, Mouse, Rat
验证活性
1. Western Blot
-Positive WB detected in: NIH/3T3 whole cell lysate, Hela whole cell lysate, HepG2 whole cell lysate, A549 whole cell lysate, RAW264.7 whole cell lysate, Rat Brain tissue
-All lanes YWHAZ antibody at 1:5000
-Secondary: Goat polyclonal to mouse IgG at 1/50000 dilution
-Predicted band size: 34 KDa
-Observed band size: 34 KDa
-Exposure time:1min
2. Western Blot
-Positive WB detected in: Hela whole cell lysate at 20μg, 10μg, 5μg, 2.5μg, 1.25μg, 0.625μg
-All lanes: YWHAZ antibody at 1:5000
-Secondary: Goat polyclonal to mouse IgG at 1/50000 dilution
-Predicted band size: 34 KDa
-Observed band size: 34 KDa
-Exposure time:5min
3. Western Blot
-Positive WB detected in: 20μg Hela whole cell lysate YWHAZ antibody at1:5000,1:10000,1:20000,1:40000,1:80000,1:160000
-Secondary: Goat polyclonal to mouse IgG at 1/50000 dilution
-Predicted band size: 34 KDa
-Observed band size: 34 KDa
-Exposure time:5min
4. IHC image of TMAH-01260 diluted at 1:200 and staining in paraffin-embedded human lung cancer tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at 37°C. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit IgG labeled by HRP and visualized using 0.05% DAB.
5. IHC image of TMAH-01260 diluted at 1:200 and staining in paraffin-embedded human liver cancer tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at 37°C. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit IgG labeled by HRP and visualized using 0.05% DAB.
6. IHC image of TMAH-01260 diluted at 1:200 and staining in paraffin-embedded human breast cancer tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at 37°C. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit IgG labeled by HRP and visualized using 0.05% DAB.
7. Immunofluorescence staining of A549 cells with TMAH-01260 at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
8. Immunofluorescence staining of Hela cells with TMAH-01260 at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
9. Immunofluorescence staining of U251 cells with TMAH-01260 at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
10. Overlay histogram showing A549 cells stained with TMAH-01260 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100. Then 10% normal goat serum was Incubated to block non-specific protein-protein interactions followed by the antibody (1µg/1*10^6 cells) for 1 h at 4°C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG(H+L) at 1/100 dilution for 30min at 4°C. Isotype control antibody (green line) was mouse IgG2b (1µg/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.
11. Overlay histogram showing Hela cells stained with TMAH-01260 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100. Then 10% normal goat serum was Incubated to block non-specific protein-protein interactions followed by the antibody (1µg/1*10^6 cells) for 1 h at 4°C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG(H+L) at 1/100 dilution for 30min at 4°C. Isotype control antibody (green line) was mouse IgG2b (1µg/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.
12. Overlay histogram showing HepG2 cells stained with TMAH-01260 (red line) at 1:100. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100. Then 10% normal goat serum was Incubated to block non-specific protein-protein interactions followed by the antibody (1µg/1*10^6 cells) for 1 h at 4°C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG(H+L) at 1/100 dilution for 30min at 4°C. Isotype control antibody (green line) was mouse IgG2b (1µg/1*10^6 cells) used under the same conditions. Acquisition of >10,000 events was performed.
13. Immunoprecipitating YWHAZ in A549 whole cell lysate
-Lane 1: Mouse control IgG2b instead of TMAH-01260 in A549 whole cell lysate.
-Lane 2: TMAH-01260 (1µg) + A549 whole cell lysate (500µg)
-Lane 3: A549 whole cell lysate (20µg)
For western blotting, the blot was detected with TMAH-01260 at 1:2000, and a HRP-conjugated Protein G antibody was used as the secondary antibody at 1:50000
14. Immunoprecipitating YWHAZ in HepG2 whole cell lysate
-Lane 1: Mouse control IgG2b instead of TMAH-01260 in HepG2 whole cell lysate.
-Lane 2: TMAH-01260 (1µg) + HepG2 whole cell lysate (500µg)
-Lane 3: HepG2 whole cell lysate (20µg)
For western blotting, the blot was detected with TMAH-01260 at 1:2000, and a HRP-conjugated Protein G antibody was used as the secondary antibody at 1:50000
应用
ELISA, WB, IHC, IF, FC
抗体种类
Monoclonal
宿主来源Mouse
亚细胞定位Cytoplasm. Melanosome. Note=Located to stage I to stage IV melanosomes.
构建方式Hybridoma Monoclonal Antibody
纯化方式Protein A purified
性状Liquid
缓冲液Preservative: 0.03% Proclin 300. Constituents: 50% Glycerol, 0.01M PBS, PH 7.4.
纯度>95%
研究背景Adapter protein implicated in the regulation of a large spectrum of both general and specialized signaling pathways. Binds to a large number of partners, usually by recognition of a phosphoserine or phosphothreonine motif. Binding generally results in the modulation of the activity of the binding partner. Induces ARHGEF7 activity on RAC1 as well as lamellipodia and membrane ruffle formation. In neurons, regulates spine maturation through the modulation of ARHGEF7 activity.
偶联与修饰
偶联
Unconjugated
抗原信息
免疫原
Recombinant Protein: Human 14-3-3 Protein zeta/delta Protein (133-212AA)
抗原种属
Human
基因ID
7534
Uniprot ID
研究领域
Others
存储&运输
储存方式Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
运输方式Shipping with blue ice.

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