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关于此项目
UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
4B7, monoclonal
Application:
immunohistochemistry
western blot
western blot
Species reactivity:
mouse, rat
Citations:
6
Technique(s):
immunohistochemistry: suitable (paraffin)
western blot: suitable
western blot: suitable
Uniprot accession no.:
产品名称
抗-IDO-1抗体,克隆4B7 | MABF850, clone 4B7, from mouse
biological source
mouse
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
4B7, monoclonal
species reactivity
mouse, rat
technique(s)
immunohistochemistry: suitable (paraffin)
western blot: suitable
isotype
IgG1κ
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Quality Level
Gene Information
mouse ... Ido1(15930)
Analysis Note
通过免疫组织化学在小鼠肾脏组织中进行评估。
免疫组织化学分析:该抗体的1:50稀释液在小鼠肾组织中检测到IDO-1。
免疫组织化学分析:该抗体的1:50稀释液在小鼠肾组织中检测到IDO-1。
Application
免疫组化分析:代表性批次的1:50稀释液在大鼠肾脏组织中检测到IDO-1。
免疫组织化学分析:代表性批次在野生型小鼠的丙酮固定冷冻结肠组织切片中检测到IDO-1免疫反应性,但在Ido1敲除小鼠中未检测到(由Lankenau医学研究所Sunil Thomas博士提供,宾夕法尼亚温尼伍德市)。
免疫荧光分析:代表性批次通过荧光免疫组织化学在野生型小鼠的丙酮固定冷冻结肠和附睾组织切片中检测到IDO-1免疫反应性,但在Ido1敲除小鼠中未检测到(由Lankenau医学研究所Sunil Thomas博士提供,宾夕法尼亚温尼伍德市)。
蛋白质印迹分析:代表性批次在野生型小鼠的附睾和结肠组织提取物中检测到 IDO-1,但在Ido1敲除小鼠中未检测到(Koduru, S., et al. (2014).J. Cell. Biochem. 115(2):391-396)。
免疫组织化学分析:代表性批次在野生型小鼠的多个丙酮固定冷冻组织切片中检测到IDO-1免疫反应性,但在Ido1敲除小鼠中未检测到,包括附睾、结肠、心脏、肝脏和4T1转移肺组织切片 (Thomas, S., et al. (2014).J. Cell. Biochem. 115(2):391-396)。
免疫组织化学分析:代表性批次在野生型小鼠的丙酮固定冷冻结肠组织切片中检测到IDO-1免疫反应性,但在Ido1敲除小鼠中未检测到(由Lankenau医学研究所Sunil Thomas博士提供,宾夕法尼亚温尼伍德市)。
免疫荧光分析:代表性批次通过荧光免疫组织化学在野生型小鼠的丙酮固定冷冻结肠和附睾组织切片中检测到IDO-1免疫反应性,但在Ido1敲除小鼠中未检测到(由Lankenau医学研究所Sunil Thomas博士提供,宾夕法尼亚温尼伍德市)。
蛋白质印迹分析:代表性批次在野生型小鼠的附睾和结肠组织提取物中检测到 IDO-1,但在Ido1敲除小鼠中未检测到(Koduru, S., et al. (2014).J. Cell. Biochem. 115(2):391-396)。
免疫组织化学分析:代表性批次在野生型小鼠的多个丙酮固定冷冻组织切片中检测到IDO-1免疫反应性,但在Ido1敲除小鼠中未检测到,包括附睾、结肠、心脏、肝脏和4T1转移肺组织切片 (Thomas, S., et al. (2014).J. Cell. Biochem. 115(2):391-396)。
该抗IDO-1抗体(克隆4B7 | MABF850)经验证可用于免疫组织化学(石蜡)、蛋白质印迹中IDO-1的检测。
Biochem/physiol Actions
克隆4B7的靶特异性已通过免疫组织化学和蛋白质印迹对野生型和Ido1敲除小鼠的组织样本进行确认(Thomas, S., et al. (2014).J. Cell. Biochem. 115(2):391-396)。
General description
吲哚胺2,3-二氧酶1(EC 1.13.11.52;UniProt P28776;也称为IDO-1、吲哚-2,3-二氧酶、吲哚胺-吡咯-2,3-二氧酶)由鼠科物种中的Ido1 (也称为Ido、Indo)基因(基因ID 15930)编码。吲哚胺2,3-二氧酶-1(IDO1)是一种含血红素的酶,在色氨酸至N-甲酰基犬尿氨酸的代谢过程中可催化限速步骤。局部色氨酸的减少和免疫调节色氨酸代谢物的上调构成IDO依赖性炎症和免疫调节的基础。据报道,IDO可通过调节组织微环境炎症反应来支持致癌作用。另据报道,IDO通过抑制T效应细胞的功能和促进T调节细胞的分化来介导癌症中的免疫逃逸。
计算分子量~45 kDa
Immunogen
KLH偶联线性肽,对应于小鼠IDO-1的N端区域。
Other Notes
浓度:请参考特定批次的数据表。
Physical form
形式:纯化
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存储类别
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Souvik Dey et al.
Journal for immunotherapy of cancer, 8(2) (2020-07-22)
The tryptophan-catabolizing enzyme indoleamine 2,3-dioxygenase 1 (IDO1), which subverts T-cell immunity at multiple levels, is itself subject to inherent T-cell reactivity. This intriguing deviation from central tolerance has been interpreted as counterbalancing IDO1-mediated immunosuppression. Based on this hypothesis, clinical studies
Yahya Jand et al.
Scientific reports, 12(1), 15963-15963 (2022-09-25)
Melatonin (MT), a neurohormone with immunomodulatory properties, is one of the metabolites produced in the brain from tryptophan (TRP) that has already strong links with the neuropathogenesis of Multiple sclerosis (MS). However, the exact molecular mechanisms behind that are not
Willy Jaya Suento et al.
Journal of neurochemistry, 157(6), 1963-1978 (2020-10-24)
Indoleamine 2,3-dioxygenase 1 (IDO1) is the first rate-limiting enzyme that metabolizes tryptophan to the kynurenine pathway. Its activity is highly inducible by pro-inflammatory cytokines and correlates with the severity of major depressive disorder (MDD). MicroRNAs (miRNAs) are involved in gene
Yuying Liu et al.
Nature communications, 8, 15207-15207 (2017-05-11)
Interactions with the immune system may lead tumorigenic cells into dormancy. However, the underlying molecular mechanism is poorly understood. Using a 3D fibrin gel model, we show that IFN-γ induces tumour-repopulating cells (TRCs) to enter dormancy through an indolamine 2,3-dioxygenase
Tatsuya Ando et al.
Molecular medicine reports, 27(2) (2022-12-10)
The partial loss of liver due to liver transplantation or acute liver failure induces rapid liver regeneration. Recently, we reported that the selective inhibition of indoleamine 2,3‑dioxygenase (Ido) 1 promotes early liver regeneration. However, the role of Ido2 in liver
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