产品: RIPK3 抗体
货号: DF10141
描述: Rabbit polyclonal antibody to RIPK3
应用: WB IF/ICC
反应: Human, Mouse
预测: Pig, Bovine, Horse, Sheep
分子量: 57 kDa; 57kD(Calculated).
蛋白号: Q9Y572
RRID: AB_2840721

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 100ul RMB¥ 2300 现货
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产品描述

来源:
Rabbit
应用:
WB 1:1000-3000, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human,Mouse
预测:
Pig(100%), Bovine(100%), Horse(100%), Sheep(100%)
克隆:
Polyclonal
特异性:
RIPK3 Antibody detects endogenous levels of total RIPK3.
RRID:
AB_2840721
引用格式: Affinity Biosciences Cat# DF10141, RRID:AB_2840721.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

Receptor interacting protein 3; Receptor interacting serine threonine kinase 3; Receptor interacting serine/threonine protein kinase 3; Receptor-interacting protein 3; Receptor-interacting serine/threonine-protein kinase 3; RIP 3; RIP like protein kinase 3; RIP-3; RIP-like protein kinase 3; RIPK 3; RIPK3; RIPK3_HUMAN;

抗原和靶标

免疫原:
Uniprot:
基因/基因ID:
表达:
Q9Y572 RIPK3_HUMAN:

Highly expressed in the pancreas. Detected at lower levels in heart, placenta, lung and kidney. Isoform 3 is significantly increased in colon and lung cancers.

序列:
MSCVKLWPSGAPAPLVSIEELENQELVGKGGFGTVFRAQHRKWGYDVAVKIVNSKAISREVKAMASLDNEFVLRLEGVIEKVNWDQDPKPALVTKFMENGSLSGLLQSQCPRPWPLLCRLLKEVVLGMFYLHDQNPVLLHRDLKPSNVLLDPELHVKLADFGLSTFQGGSQSGTGSGEPGGTLGYLAPELFVNVNRKASTASDVYSFGILMWAVLAGREVELPTEPSLVYEAVCNRQNRPSLAELPQAGPETPGLEGLKELMQLCWSSEPKDRPSFQECLPKTDEVFQMVENNMNAAVSTVKDFLSQLRSSNRRFSIPESGQGGTEMDGFRRTIENQHSRNDVMVSEWLNKLNLEEPPSSVPKKCPSLTKRSRAQEEQVPQAWTAGTSSDSMAQPPQTPETSTFRNQMPSPTSTGTPSPGPRGNQGAERQGMNWSCRTPEPNPVTGRPLVNIYNCSGVQVGDNNYLTMQQTTALPTWGLAPSGKGRGLQHPPPVGSQEGPKDPEAWSRPQGWYNHSGK

种属预测

种属预测:

score>80的预测可信度较高,可尝试用于WB检测。*预测模型主要基于免疫原序列比对,结果仅作参考,不作为质保凭据。

Species
Results
Score
Pig
100
Horse
100
Bovine
100
Sheep
100
Dog
0
Xenopus
0
Zebrafish
0
Chicken
0
Rabbit
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

翻译修饰 - Q9Y572 作为底物

Site PTM Type Enzyme
K5 Ubiquitination
K55 Ubiquitination
T182 Phosphorylation
S199 Phosphorylation Q9Y572 (RIPK3)
T224 Phosphorylation
S227 Phosphorylation Q9Y572 (RIPK3)
S241 Phosphorylation
T252 Phosphorylation
S299 Phosphorylation
T300 Phosphorylation
S316 Phosphorylation
S320 Phosphorylation
T325 Phosphorylation
S339 Phosphorylation
S359 Phosphorylation
K363 Ubiquitination
S372 Phosphorylation
S410 Phosphorylation
T412 Phosphorylation
R486 Methylation

翻译修饰 - Q9Y572 作为激酶

Substrate Site Source
Q8NB16 (MLKL) T357 Uniprot
Q8NB16 (MLKL) S358 Uniprot
Q9UER7 (DAXX) S668 Uniprot
Q9Y572 (RIPK3) S199 Uniprot
Q9Y572 (RIPK3) S227 Uniprot

研究背景

功能:

Essential for necroptosis, a programmed cell death process in response to death-inducing TNF-alpha family members. Upon induction of necrosis, RIPK3 interacts with, and phosphorylates RIPK1 and MLKL to form a necrosis-inducing complex. RIPK3 binds to and enhances the activity of three metabolic enzymes: GLUL, GLUD1, and PYGL. These metabolic enzymes may eventually stimulate the tricarboxylic acid cycle and oxidative phosphorylation, which could result in enhanced ROS production.

翻译修饰:

RIPK1 and RIPK3 undergo reciprocal auto- and trans-phosphorylation. Phosphorylation of Ser-199 plays a role in the necroptotic function of RIPK3. Phosphorylation at Ser-227 is required for binding MLKL. Phosphorylation at Thr-182 is important for its kinase activity, interaction with PELI1 and PELI1-mediated 'Lys-48'-linked polyubiquitination and for its ability to mediate TNF-induced necroptosis.

Polyubiquitinated with 'Lys-48' and 'Lys-63'-linked chains by BIRC2/c-IAP1 and BIRC3/c-IAP2, leading to activation of NF-kappa-B. Polyubiquitinated with 'Lys-48'-linked chains by PELI1 leading to its subsequent proteasome-dependent degradation. Ubiquitinated by STUB1 leading to its subsequent proteasome-dependent degradation.

细胞定位:

Cytoplasm>Cytosol. Cell membrane. Mitochondrion.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
组织特异性:

Highly expressed in the pancreas. Detected at lower levels in heart, placenta, lung and kidney. Isoform 3 is significantly increased in colon and lung cancers.

亚基结构:

Interacts (via RIP homotypic interaction motif) with RIPK1 (via RIP homotypic interaction motif); this interaction induces RIPK1 phosphorylation and formation of a RIPK1-RIPK3 necrosis-inducing complex. Upon TNF-induced necrosis, the RIPK1-RIPK3 dimer further interacts with PGAM5 and MLKL; the formation of this complex leads to PGAM5 phosphorylation and increase in PGAM5 phosphatase activity. Interacts with MLKL; the interaction is direct. Binds TRAF2 and is recruited to the TNFR-1 signaling complex. Interacts with PYGL, GLUL and GLUD1; these interactions result in activation of these metabolic enzymes. Interacts with BIRC2/c-IAP1, BIRC3/c-IAP2 and XIAP/BIRC4. Interacts with ARHGEF2. Interacts with PELI1 (via atypical FHA domain); the phosphorylated form at Thr-182 binds preferentially to PELI1. Interacts with BUB1B, TRAF2 and STUB1. Interacts with ZBP1 (By similarity).

蛋白家族:

Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family.

研究领域

· Cellular Processes > Cell growth and death > Necroptosis.   (View pathway)

· Environmental Information Processing > Signal transduction > TNF signaling pathway.   (View pathway)

· Organismal Systems > Immune system > NOD-like receptor signaling pathway.   (View pathway)

· Organismal Systems > Immune system > Cytosolic DNA-sensing pathway.   (View pathway)

文献引用

1). HNEAP Regulates Necroptosis of Cardiomyocytes by Suppressing the m5 C Methylation of Atf7 mRNA. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023 (PubMed: 37870216) [IF=15.1]

Application: WB    Species: Mouse    Sample: cardiomyocytes

Figure 2 Knockdown of HNEAP attenuates H/R‐induced cardiomyocyte necroptosis. a–d) The isolated neonatal mice cardiomyocytes were transfected with HNEAP agomir (HNEAP) or its negative control (NC) for 24 h. a) The expression level of HNEAP was analyzed by qPCR (n = 6 independent experiments). b) Necroptosis was determined by the PI staining. DAPI indicates Nucleus. Bar = 25 µm. c) Quantitative analysis of the percentage of necroptotic cells (n = 6 independent experiments). d) The activity of lactate dehydrogenase (LDH) in cardiomyocytes after transfection with HNEAP or NC. (n = 6 independent experiments). e) The isolated neonatal mice cardiomyocytes were transfected with HNEAP antagomir (anta) or its negative control (anta‐NC) for 24 h. The expression level of HNEAP was analyzed by qPCR (n = 4 independent experiments). f–i) The isolated neonatal mice cardiomyocytes were transfected with HNEAP antagomir (anta) or its negative control (anta‐NC) for 24 h and then cells were treated with H/R as described in the Experimental Section. f) qPCR analysis of the expression level of HNEAP (n = 5 independent experiments). g) Necroptosis was determined by the PI staining. DAPI indicates Nucleus. Bar = 25 µm. h) Quantitative analysis of the percentage of necroptotic cells (n = 6 independent experiments). i) The upper panel shows the activity of LDH in cardiomyocytes after transfection with anta or anta‐NC and treated with H/R (n = 6 independent experiments). The lower panel is representative western blot showing the expression of RIPK1 and RIPK3. Data are presented as Mean ± SD. All data were analyzed using one‐way ANOVA.

2). Early Protection by Resveratrol in Rat Lung Transplantation. MEDICAL SCIENCE MONITOR, 2019 (PubMed: 30684444) [IF=3.1]

Application: IHC    Species: rat    Sample: lung

Figure 5.| Immunohistochemistry of RIPK3, MLKL, and TNF-a in lung grafts or in situ. The magnification of pictures is 400× (A). Protein expression was assessed as positive immune response or negative immune response depending on the immunohistochemistry score of different groups (NS group: n=8; DEM group: n=7; RES group: n=8). Positive immune response slices had more brown-staining cells in particular areas than the negative ones (B–D).

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