RAB0978
Phosphotyrosine CSF1R / Macrophage Colony-stimulating Factor 1 Receptor ELISA Kit
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1 KIT
R$ 3.289,00
R$ 3.289,00
Previsão de entrega em26 de abril de 2025
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1 KIT
R$ 3.289,00
About This Item
Código UNSPSC:
41116158
NACRES:
NA.32
R$ 3.289,00
Previsão de entrega em26 de abril de 2025
Produtos recomendados
reatividade de espécies
human
técnica(s)
ELISA: suitable
assay range
inter-assay cv: <10%
intra-assay cv: <12%
Condições de expedição
wet ice
temperatura de armazenamento
−20°C
Informações sobre genes
human ... CSF1R(1436)
Descrição geral
CSF1R (colony stimulating factor 1 receptor) or FMS, acts as a receptor for CSF1 and regulates monocyte and macrophage functioning. It is a member of the platelet-derived growth factor (PDGF) family of proteins and is a type III RTK (receptor tyrosine kinase). CSF1R is composed of five immunoglobulin (Ig)-like domains, a transmembrane region, a juxtamembrane domain and kinase insert domain (KID) intersecting the kinase domain.[1][2]
The antibody pair provided in this kit recognizes Human Tyrosine-Phosphorylated-MCSFR.
Aplicação
For research use only. Not for use in diagnostic procedures.
Please refer to the attached General ELISA KIT Procedure (sandwich, competitive & Indirect ELISA)
Please refer to the attached General ELISA KIT Procedure (sandwich, competitive & Indirect ELISA)
Ações bioquímicas/fisiológicas
CSF1R (colony stimulating factor 1 receptor) and its ligand CSF1 are linked to poor prognosis in patients with solid tumors and in patients with female reproductive cancers. In breast cancers with decreased claudin levels, this protein regulates the switch between proliferative and invasive state of the tumor, acting downstream of TGFβ (tumor growth factor β). Haploinsufficiency in this receptor might lead to aberration of microglial function, which might be a contributor to the pathogenesis of hereditary diffuse leukoencephalopathy with spheroids (HDLS).[2][3][4]
Componentes do kit também disponíveis separadamente
Nº do produto
Descrição
SDS
- RABHRP6Phosphotyrosine ELISA HRP-StreptavidinSDS
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Met. Corr. 1
Código de classe de armazenamento
8A - Combustible corrosive hazardous materials
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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Certificados de análise (COA)
Lot/Batch Number
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Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
CSF1R mutations in hereditary diffuse leukoencephalopathy with spheroids are loss of function.
Pridans C, et al.
Scientific Reports, (3), 3013-3013 (2013)
Takuya Konno et al.
Neurology, 82(2), 139-148 (2013-12-18)
To clarify the genetic, clinicopathologic, and neuroimaging characteristics of patients with hereditary diffuse leukoencephalopathy with spheroids (HDLS) with the colony stimulating factor 1 receptor (CSF-1R) mutation. We performed molecular genetic analysis of CSF-1R in patients with HDLS. Detailed clinical and
A Patsialou et al.
Oncogene, 34(21), 2721-2731 (2014-08-05)
Patient data suggest that colony-stimulating factor-1 (CSF1) and its receptor (CSF1R) have critical roles during breast cancer progression. We have previously shown that in human breast tumors expressing both CSF1 and CSF1R, invasion in vivo is dependent both on a
Parag P Patwardhan et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 20(12), 3146-3158 (2014-04-11)
Malignant peripheral nerve sheath tumor (MPNST) is a highly aggressive tumor type that is resistant to chemotherapy and there are no effective therapies. MPNSTs have been shown to have gene amplification for receptor tyrosine kinases (RTK), PDGFR and c-Kit. We
V Barbetti et al.
Oncogene, 33(34), 4359-4364 (2013-12-24)
The colony-stimulating factor-1 (CSF-1) and its receptor CSF-1R physiologically regulate the monocyte/macrophage system, trophoblast implantation and breast development. An abnormal CSF-1R expression has been documented in several human epithelial tumors, including breast carcinomas. We recently demonstrated that CSF-1/CSF-1R signaling drives
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