推薦產品
生物源
mouse
品質等級
抗體表格
purified immunoglobulin
抗體產品種類
primary antibodies
無性繁殖
4E12, monoclonal
物種活性
human
濃度
1 mg/mL
技術
activity assay: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable
同型
IgG2aκ
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
目標翻譯後修改
unmodified
基因資訊
human ... VASH1(22846)
一般說明
Vasohibin-1 is an endothelium-derived negative feedback regulator of angiogenesis. Vasohibin-1 inhibited migration, proliferation, and network formation by ECs in culture, as well as angiogenesis in vivo, and Vasohibin-1 was selective for endothelial cells and its influence was eliminated by hypoxia or TNF-alpha interaction. Vasohibin is preferentially expressed in endothelial cells and does not appear to promote proliferation or tumor growth when over expressed. Vasohibin-1 expression is induced by VEGF expression and its effects are mediated through VEGF-R2 independent of VEGF-R1 and Vasohibin-1 may directly influence the expression of VEGF-R2. Because the inhibition effects of Vasohibin-1 are nullified by hypoxia and various cytokines it is thought that this is how tumors escape this built-in negative regulator of angiogenesis. Vasohibin-1 is highly expressed in fetal organs and the endothelial cells during development, and also expressed in the brain and placental and microvessels endothelial cells of atherosclerotic lesions in the adult.
免疫原
KLH-conjugated linear peptide corresponding to Human Vasohibin-1.
應用
Functional Activity Assay: A representative lot of this antibody induced cellular senescence (Miyashita, H., et al. (2012) PLOS ONE. 7(10):e46459).
Western Blotting Analysis: A representative lot of this antibody detected Vasohibin-1 in HUVECs transfected with control siRNA, but not in HUVECs transfected with Vasohibin-1 siRNA (Miyashita, H., et al. (2012) PLOS ONE. 7(10):e46459).
Western Blotting Analysis: A representative lot of this antibody detected Vasohibin-1 (KIAA1036 protein referenced in publication) in VEGF-stimulated HUVECs and GM7373 transfected cell lysate (Watanabe, K,, et al. (2004) JCI. 114(7):898-907).
Immunohistochemistry Analysis: A representative lot of this antibody detected Vasohibin-1 (KIAA1036 protein referenced in publication) in human placenta tissue (Watanabe, K,, et al. (2004) JCI. 114(7):898-907).
Immunocytochemistry Analysis: A representative lot of this antibody detected Vasohibin-1 (KIAA1036 protein referenced in publication) in HUVEC cells (Watanabe, K,, et al. (2004) JCI. 114(7):898-907).
Western Blotting Analysis: A representative lot of this antibody detected Vasohibin-1 in HUVECs transfected with control siRNA, but not in HUVECs transfected with Vasohibin-1 siRNA (Miyashita, H., et al. (2012) PLOS ONE. 7(10):e46459).
Western Blotting Analysis: A representative lot of this antibody detected Vasohibin-1 (KIAA1036 protein referenced in publication) in VEGF-stimulated HUVECs and GM7373 transfected cell lysate (Watanabe, K,, et al. (2004) JCI. 114(7):898-907).
Immunohistochemistry Analysis: A representative lot of this antibody detected Vasohibin-1 (KIAA1036 protein referenced in publication) in human placenta tissue (Watanabe, K,, et al. (2004) JCI. 114(7):898-907).
Immunocytochemistry Analysis: A representative lot of this antibody detected Vasohibin-1 (KIAA1036 protein referenced in publication) in HUVEC cells (Watanabe, K,, et al. (2004) JCI. 114(7):898-907).
Research Category
Apoptosis & Cancer
Apoptosis & Cancer
Research Sub Category
Tumor Markers
Tumor Markers
This Anti-Vasohibin-1 Antibody, clone 4E12 (Azide Free) is validated for use in Western Blotting and Immunohistochemistry and Immunocytochemistry and Activity Assay for the detection of Vasohibin-1.
品質
Evaluated by Western Blotting in HEK293 cell lysate.
Western Blotting Analysis: 1 µg/mL of this antibody detected Vasohibin-1 in 10 µg of HEK293 cell lysate.
Western Blotting Analysis: 1 µg/mL of this antibody detected Vasohibin-1 in 10 µg of HEK293 cell lysate.
標靶描述
~ 41 kDa observed
外觀
Protein G Purified
Format: Purified
Purified mouse monoclonal IgG2aκ in buffer containing PBS without preservatives.
儲存和穩定性
Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
Kazuhide Watanabe et al.
The Journal of clinical investigation, 114(7), 898-907 (2004-10-07)
Negative feedback is a crucial physiological regulatory mechanism, but no such regulator of angiogenesis has been established. Here we report a novel angiogenesis inhibitor that is induced in endothelial cells (ECs) by angiogenic factors and inhibits angiogenesis in an autocrine
Hiroki Miyashita et al.
PloS one, 7(10), e46459-e46459 (2012-10-12)
Vasohibin-1 (VASH1) is isolated as an endothelial cell (EC)-produced angiogenesis inhibitor. We questioned whether VASH1 plays any role besides angiogenesis inhibition, knocked-down or overexpressed VASH1 in ECs, and examined the changes of EC property. Knock-down of VASH1 induced premature senescence
Siem van der Laan et al.
Cell reports, 29(12), 4159-4171 (2019-12-19)
The two related members of the vasohibin family, VASH1 and VASH2, encode human tubulin detyrosinases. Here we demonstrate that, in contrast to VASH1, which requires binding of small vasohibin binding protein (SVBP), VASH2 has autonomous tubulin detyrosinating activity. Moreover, we
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