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Anti-OCT4 Antibody (7S23)

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产品编号 TMAH-00842

Anti-OCT4 Antibody (7S23) 是一种 Mouse 抗体,靶向 OCT4。Anti-OCT4 Antibody (7S23) 可用于 ELISA, WB, IHC, IF, FC。

Anti-OCT4 Antibody (7S23)

Anti-OCT4 Antibody (7S23)

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产品编号 TMAH-00842

Anti-OCT4 Antibody (7S23) 是一种 Mouse 抗体,靶向 OCT4。Anti-OCT4 Antibody (7S23) 可用于 ELISA, WB, IHC, IF, FC。

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产品介绍

生物活性
产品描述
Anti-OCT4 Antibody (7S23) is a Mouse antibody targeting OCT4. Anti-OCT4 Antibody (7S23) can be used in ELISA, WB, IHC, IF, FC.
Ig Type
IgG2b
克隆号
7S23
交叉反应
Human, Mouse, Rat
验证活性
1. Western Blot
-Positive WB detected in: HepG2 whole cell lysate
-All lanes: OCT4 antibody at 1:500
-Secondary: Goat polyclonal to Mouse IgG at 1/10000 dilution
-Predicted band size: 39, 31 kDa
-Observed band size: 45 kDa
2. Western Blot
-Positive WB detected in: Mouse brain tissue, Rat brain tissue
-All lanes: OCT4 antibody at 1:1000, 1:5000, 1:8000
-Secondary: Goat polyclonal to Mouse IgG at 1/10000 dilution
-Predicted band size: 39, 31 kDa
-Observed band size: 45 kDa
3. IHC image of TMAH-00842 diluted at 1:100 and staining in paraffin-embedded human lung cancer 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 RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
4. IHC image of TMAH-00842 diluted at 1:100 and staining in paraffin-embedded human testis 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 RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
5. IHC image of TMAH-00842 diluted at 1:100 and staining in paraffin-embedded human colon cancer 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 RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
6. IHC image of TMAH-00842 diluted at 1:100 and staining in paraffin-embedded human endometrial cancer 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 RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
7. Immunofluorescence staining of A549 cells with TMAH-00842 at 1:100, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).
8. Immunofluorescence staining of Ntera-2 cells with TMAH-00842 at 1:100, counter-stained with DAPI. The cells were blocked in 10% normal Goat Serum and then incubated with the primary antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L).
9. Overlay histogram showing A549 cells stained with TMAH-00842 (red line) at 1:100. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
10. Overlay histogram showing Ntera-2 cells stained with TMAH-00842 (red line) at 1:100. The cells were incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by primary antibody for 1 h at 4°C. The secondary antibody used was FITC goat anti-mouse IgG(H+L) at 1/200 dilution for 1 h at 4°C. Isotype control antibody (green line) was used under the same conditions. Acquisition of >10,000 events was performed.
应用
ELISA, WB, IHC, IF, FC
抗体种类
Monoclonal
宿主来源Mouse
亚细胞定位Cytoplasm. Nucleus.
构建方式Hybridoma Monoclonal Antibody
纯化方式Protein G 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Transcription factor that binds to the octamer motif (5'-ATTTGCAT-3'). Forms a trimeric complex with SOX2 or SOX15 on DNA and controls the expression of a number of genes involved in embryonic development such as YES1, FGF4, UTF1 and ZFP206. Critical for early embryogenesis and for embryonic stem cell pluripotency.
偶联与修饰
偶联
Unconjugated
抗原信息
免疫原
Recombinant Human POU domain, class 5, transcription factor 1 protein (1-360AA)
抗原种属
Human
基因ID
5460
Uniprot ID
研究领域
Epigenetics and Nuclear Signaling
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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