Anti-TRIM32 抗体 [EP6355]
Anti-TRIM32 antibody [EP6355]
- RabMAb
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(3 Publications)
Rabbit Monoclonal TRIM32 antibody. Suitable for WB and reacts with Human samples. Cited in 3 publications.
別名を表示する
HT2A, TRIM32, E3 ubiquitin-protein ligase TRIM32, 72 kDa Tat-interacting protein, RING-type E3 ubiquitin transferase TRIM32, Tripartite motif-containing protein 32, Zinc finger protein HT2A
- WB
Supplier Data
Western blot - Anti-TRIM32 antibody [EP6355] (AB131223)
The bands above 75kDa are ubiquitination bands which was described in the literature (PMID : 30884854, 16243356, 21628460). Blocking buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-TRIM32 antibody [EP6355] (ab131223) at 1/2000 dilution
All lanes:
Human skeletal muscle lysate at 15 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 73 kDa
false
Exposure time: 60s
- WB
Supplier Data
Western blot - Anti-TRIM32 antibody [EP6355] (AB131223)
Although some papers support the expression of TRIM32 in SK-BR-3, T-47D, MCF7, MDA-MB-435S, MD-MB-468 (PMID : 29721043), ab131223 can’t detect monomer TRIM32 band of interest in these cell lines. The bands above 75kDa are ubiquitination bands which was described in the literature (PMID : 30884854, 16243356, 21628460). Blocking buffer and concentration : 5% NFDM/TBST. Exposure time : Lane 1 & Lane 2 : 3 seconds; Lane 3- Lane7 : 180 seconds.
All lanes:
Western blot - Anti-TRIM32 antibody [EP6355] (ab131223) at 1/200 dilution
Lane 1:
293T (Human embryonic kidney epithelial cell) transfected with an empty vector (vector control), containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 2:
293T transfected with TRIM32 expression vector containing a myc-His-tag®, whole cell lysate at 20 µg
Lane 3:
SK-BR-3 (Human breast adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 4:
T-47D (Human ductal breast epithelial tumor epithelial cell) whole cell lysate at 20 µg
Lane 5:
MCF7 (Human breast adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 6:
NCI-H460 (Human Large Cell Lung Cancer epithelial cell) whole cell lysate at 20 µg
Lane 7:
Human skeletal muscle lysate at 20 µg
false
- OI-RD Scanning
Unknown
OI-RD Scanning - Anti-TRIM32 antibody [EP6355] (AB131223)
We have systematically measured KD (the equilibrium dissociation constant between the antibody and its antigen), of more than 840 recombinant antibodies to assess not only their individual KD values but also to see the average affinity of antibody. Based on the comparison with published literature values for mouse monoclonal antibodies, Recombinant antibodies appear to be on average 1-2 order of magnitude higher affinity.
Reactivity data
製品の詳細
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Species reactivity
Rat: We have preliminary internal testing data to indicate this antibody may not react with this species.
Please contact us for more information.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存期間
短期保存温度
長期保存温度
分注に関する情報
保管に関する情報
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
TRIM32 participates in regulating muscle cell differentiation and proliferation. It interacts with several proteins including dysbindin and myospryn suggesting its involvement in a multi-protein complex. TRIM32 has a regulatory role in muscle maintenance where it influences the stability and function of muscle proteins. Moreover it is also involved in neurogenesis affecting neuronal differentiation and survival emphasizing its role beyond muscle tissues.
Pathways
TRIM32 plays a significant role in the PI3K/Akt signaling pathway and the TGF-beta signaling pathway. In the PI3K/Akt pathway TRIM32 modulates cell growth and survival interacting with proteins such as Akt and mTOR. In the context of TGF-beta signaling TRIM32 can influence cellular processes like proliferation and differentiation possibly by interacting with SMAD proteins. These interactions indicate its importance in cellular growth and differentiation pathways.
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ターゲットの情報
文献 (3)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 11:6316 PubMed33298911
2020
Applications
Unspecified application
Species
Unspecified reactive species
eLife 7: PubMed30281021
2018
Applications
Unspecified application
Species
Unspecified reactive species
PLoS pathogens 12:e1005584 PubMed27082114
2016
Applications
Unspecified application
Species
Unspecified reactive species
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