RPGRIP1L Antibody
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中文名稱：RPGRIP1L兔多克隆抗體
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貨號：CSB-PA020101GA01HU
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規格：￥3,900
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其他：
產品詳情
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Uniprot No.：
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基因名：RPGRIP1L
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別名：CORS 3 antibody; CORS3 antibody; Fantom antibody; FTM antibody; FTM_HUMAN antibody; JBTS 1 antibody; JBTS 7 antibody; JBTS1 antibody; JBTS7 antibody; Joubert syndrome 1 antibody; Joubert syndrome 7 antibody; Meckel syndrome; type 1 antibody; Meckel syndrome; type 5 antibody; MKS 5 antibody; MKS5 antibody; Nephrocystin-8 antibody; NPHP 8 antibody; NPHP8 antibody; Protein fantom antibody; Retinitis pigmentosa GTPase regulator interacting protein 1 like antibody; RPGR interacting protein 1 like protein antibody; RPGR-interacting protein 1-like protein antibody; RPGRIP1 like protein antibody; RPGRIP1-like protein antibody; Rpgrip1l antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Human RPGRIP1L
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免疫原種屬：Homo sapiens (Human)
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抗體亞型：IgG
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純化方式：Antigen Affinity purified
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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產品提供形式：Liquid
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應用范圍：ELISA,WB
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Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期：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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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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功能：Negatively regulates signaling through the G-protein coupled thromboxane A2 receptor (TBXA2R). May be involved in mechanisms like programmed cell death, craniofacial development, patterning of the limbs, and formation of the left-right axis. Involved in the organization of apical junctions; the function is proposed to implicate a NPHP1-4-8 module. Does not seem to be strictly required for ciliogenesis. Involved in establishment of planar cell polarity such as in cochlear sensory epithelium and is proposed to implicate stabilization of disheveled proteins. Involved in regulation of proteasomal activity at the primary cilium probably implicating association with PSDM2.
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基因功能參考文獻：
- we didn't found the significant association between RPGRIP1L and BMI in Chinese women PMID: 29657248
- our studies revealed RPGRIP1L as a novel MyoVa-binding protein - the first to be demonstrated to interact with MyoVa at the centrosome - and uncover an unprecedented link between MyoVa and ciliogenesis, providing new perspectives for studies aiming to better understand why defects in MyoVa cause neurological disorders in Griscelli syndrome patients. PMID: 28266547
- Importantly, one Japanese and one Omani families carried compound biallelic mutations in two distinct genes (TMEM67/RPGRIP1L and TMEM138/BBS1, respectively). PMID: 27434533
- KIAA1005 (rs3213758)is associated with single nucleotide polymorphisms in Korean patients, either non-segmental or segmental type. PMID: 23678272
- All Spanish families with Alstrom syndrome were homozygous for 229A allele of RPGRIP1L, with the exception of a p.A229T heterozygous patient. PMID: 22876109
- First evidence of the association between RPGRIP1L gene and susceptibility of Vascular Dementia. PMID: 22425971
- Genetic variation may affect severity of disease for X-linked retinitis pigmentosa. PMID: 22183348
- Data show that the minor allele (N) of I393N in IQCB1 and the common allele (R) of R744Q in RPGRIP1L were associated with severe disease in XlRP with RPGR mutations. PMID: 21857984
- Nek4 interaction with both RPGRIP1 and the RPGRIP1L is involved in cilium assembly. PMID: 21685204
- Insulin was identified as a key factor regulating FTM expression during human preadipocyte differentiation. PMID: 20865646
- CSPP isoforms require their common C-terminal domain to interact with Nephrocystin 8 (NPHP8/RPGRIP1L) and to form a ternary complex with NPHP8 and NPHP4. PMID: 20519441
- RPGRIP1L interacts with retinitis pigmentosa GTPase, loss of which causes retinal degeneration. PMID: 19430481
- Mutations in MKS3 are responsible for the majority of COACH syndrome, with minor contributions from CC2D2A and RPGRIP1L. PMID: 19574260
- Responsible for Joubert syndrome, affecting cilia and basal bodies. PMID: 17558407
- Mutations can cause the multiorgan phenotypic abnormalities found in cerebello-oculo-renal syndrome or Meckel syndrome. PMID: 17558409
- T615P mutation represents the most common mutation in the RPGRIP1L gene causing disease in about 8-10% of Joubert syndrome type B patients negative for NPHP1, NPHP6, or AHI1 mutations PMID: 17960139
- Discuss Fto/Ftm gene expression regulation via CUTL1. PMID: 18256137
- Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies. Review. PMID: 18281315
- RPGRIP1L mutations are largely confined to the cerebello-renal subgroup, while they overall represent a rare cause of JSRD (<2%). PMID: 18565097
- data suggest that RPGRIP1L suppresses anchorage-independent growth partly through the mitotic checkpoint protein Mad2. PMID: 19410446
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相關疾病：Joubert syndrome 7 (JBTS7); Meckel syndrome 5 (MKS5); COACH syndrome (COACHS)
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亞細胞定位：Cytoplasm. Cytoplasm, cytoskeleton, cilium basal body. Cytoplasm, cytoskeleton, cilium axoneme. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cell junction, tight junction.
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蛋白家族：RPGRIP1 family
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組織特異性：Ubiquitously expressed with relatively high level of expression in hypothalamus and islet. During early development, expressed in multiple organs including brain, eye, forelimb and kidney.
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數據庫鏈接：
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