重组Alexa Fluor® 488荧光Anti-Hamartin抗体[EP318Y]
Alexa Fluor® 488 Anti-Hamartin antibody [EP318Y]
- BOND RX™ Validated
- RabMAb
- Recombinant
- 了解详情
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Rabbit Recombinant Monoclonal Hamartin antibody - conjugated to Alexa Fluor® 488. Suitable for IHC-P, Flow Cyt (Intra) and reacts with Human samples.
查看别名
KIAA0243, TSC, TSC1, Hamartin, Tuberous sclerosis 1 protein
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Alexa Fluor® 488 Anti-Hamartin antibody [EP318Y] (AB223387)
Overlay histogram showing HeLa cells stained with ab223387 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Triton X-100 for 15 min. The cells were then incubated in 1x PBS / 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (ab223387, 1/50 dilution) for 30 min at 22°C.
Isotype control antibody (black line) was Rabbit IgG (monoclonal) Alexa Fluor® 488 (ab199091) used at the same concentration and conditions as the primary antibody. Unlabelled sample (blue line) was also used as a control.
Acquisition of >5,000 events were collected using a 50 mW Blue laser (488nm) and 530/30 bandpass filter.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 488 Anti-Hamartin antibody [EP318Y] (AB223387)
IHC image of Hamartin staining in a section of formalin-fixed paraffin-embedded normal human kidney*.
The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20mins performed on a Leica BOND™. Non-specific protein-protein interactions were then blocked in TBS containing 0.025% (v/v) Triton X-100, 0.3M (w/v) glycine and 1% (w/v) BSA for 1h at room temperature. The section was then incubated overnight at +4°C in TBS containing 0.025% (v/v) Triton X-100 and 1% (w/v) BSA with ab223387 at 1/100 dilution (shown in green) and counterstained using ab195884, Rat monoclonal to Tubulin (Alexa Fluor® 647), at 1/250 dilution (shown in red). Nuclear DNA was labelled with DAPI (shown in blue). The section was then mounted using Fluoromount®.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
For other IHC staining systems (automated and non-automated), customers should optimize variable parameters such as antigen retrieval conditions, antibody concentrations and incubation times.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.
不同偶联物与剂型 (10)
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Anti-Hamartin antibody [EP318Y]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-Hamartin antibody [EP318Y]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-Hamartin antibody [EP318Y]
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Anti-Hamartin antibody [EP318Y] - BSA and Azide free
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660 APC
APC Anti-Hamartin antibody [EP318Y]
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HRP Anti-Hamartin antibody [EP318Y]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-Hamartin antibody [EP318Y]
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-Hamartin antibody [EP318Y]
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578 PE
PE Anti-Hamartin antibody [EP318Y]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-Hamartin antibody [EP318Y]
反应性数据
产品详情
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存时间
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Hamartin functions as part of the TSC1-TSC2 complex which acts as a tumor suppressor. This complex inhibits the mechanistic target of rapamycin complex 1 (mTORC1) an essential regulator of cell growth proliferation and protein synthesis. Through this regulation Hamartin plays a critical role in maintaining cellular homeostasis and preventing abnormal cell growth that can lead to tumorigenesis.
Pathways
Hamartin is integral to the mTOR signaling pathway an important pathway that regulates cell metabolism growth and survival. This pathway involves the interaction of Hamartin with Tuberin (TSC2) helping to control the activation of mTORC1. Additionally Hamartin is involved in the PI3K/Akt signaling pathway which further influences mTOR activity and cellular responses to growth factors.
产品实验方案
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靶点信息
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