PLD3 Antibody
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货号:CSB-PA018146LA01HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) PLD3 Polyclonal antibody
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Uniprot No.:Q8IV08
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基因名:
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别名:Choline phosphatase 3 antibody; HindIII K4L homolog antibody; HU K4 antibody; Hu-K4 antibody; HUK4 antibody; Phosphatidylcholine hydrolyzing phospholipase D3 antibody; Phosphatidylcholine-hydrolyzing phospholipase D3 antibody; Phospholipase D family; member 3 antibody; Phospholipase D3 antibody; PLD 3 antibody; PLD3 antibody; PLD3_HUMAN antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Phospholipase D3 protein (70-176AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,PLD3 Antibody (CSB-PA018146LA01HU),的标记方式是Non-conjugated。对于PLD3 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, IHC, IF
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推荐稀释比:
Application Recommended Dilution IHC 1:20-1:200 IF 1:50-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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靶点详情
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功能:5'->3' DNA exonuclease which digests single-stranded DNA (ssDNA). Regulates inflammatory cytokine responses via the degradation of nucleic acids, by reducing the concentration of ssDNA able to stimulate TLR9, a nucleotide-sensing receptor in collaboration with PLD4. May be important in myotube formation. Plays a role in lysosomal homeostasis. Involved in the regulation of endosomal protein sorting.
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基因功能参考文献:
- Data show that phospholipase D3 (PLD3) functions in endosomal protein sorting and plays an important role in regulating amyloid precursor protein (APP) processing. PMID: 29368044
- PLD3 variant V232M was associated with Alzheimer's disease risk in overall sample sets. PMID: 26189833
- main findings of our this provide evidence that support the possible role of PLD3 common variants in influencing AD-related neuroimaging phenotypes. PMID: 26232066
- Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort PMID: 26411346
- one PLD3 variant (rs11667768) was associated with amyloid burden detected by CSF in normal individuals, suggesting the potential role of PLD3 in Abeta pathology PMID: 26402410
- The rare coding variant might not play an important role in AD risk in mainland China. PMID: 24866402
- genetic and functional data indicate that carriers of PLD3 coding variants have a twofold increased risk for late-onset Alzheimer's disease and that PLD3 influences APP processing PMID: 24336208
- PLD3 localizes to lysosomes PMID: 21752829
- PLD3 overexpression may inhibit Akt phosphorylation and further block the transduction of insulin signaling in C2C12 cells. PMID: 20112697
- Our data do not support the hypothesis that the HindIII(+/-) site of the Y chromosome is a marker of cardiovascular risk in white men, highlighting the need for replication in genetic association studies. PMID: 16580565
- receptor stimulation leads to sequestration of recycling endosomes in a classical protein kinase C- and phospholipase D-dependent manner PMID: 19525236
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相关疾病:Genetic variants in PLD3 have been suggested to be associated with an increased risk for Alzheimer disease (PubMed:24336208, PubMed:25832409). Further studies, however, did not support PLD3 involvement in this disease (PubMed:25832408, PubMed:25832411, PubMed:25832413, PubMed:25832410, PubMed:26411346).
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亚细胞定位:Endoplasmic reticulum membrane; Single-pass type II membrane protein. Lysosome lumen. Early endosome membrane; Single-pass type II membrane protein. Late endosome membrane; Single-pass type II membrane protein. Golgi apparatus membrane; Single-pass type II membrane protein. Endosome membrane; Single-pass type II membrane protein.
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蛋白家族:Phospholipase D family
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组织特异性:Widely expressed. In the brain, high levels of expression are detected in the frontal, temporal and occipital cortices and hippocampus. Expressed at low level in corpus callosum.
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数据库链接:
HGNC: 17158
OMIM: 615698
KEGG: hsa:23646
STRING: 9606.ENSP00000348901
UniGene: Hs.257008
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