货号：14-530M

品牌：Merck Millipore

规格：250Ug

目录价：￥41939.00

市场价格：￥35648.15

会员价格：￥33551.20

金山科研平台，产品价格货期咨询微信：jinshanbio Description: B-Raf (δ1-415), active View All» Trade Name: Upstate (Millipore) View All» Qty/Pk: 250 µg View All» Product Overview: N-terminal GST-tagged recombinant human B-Raf residues 416-end View All» Key Applications: Kinase Assay View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» UniProt Summary: FUNCTION: SwissProt: P15056 # Involved in the transduction of mitogenic signals from the cell membrane to the nucleus. May play a role in the postsynaptic responses of hippocampal neuron.COFACTOR: Binds 2 zinc ions per subunit (By similarity).SIZE: 766 amino acids; 84437 Da SUBUNIT: Interacts with RIT1 (By similarity).SUBCELLULAR LOCATION: Cytoplasm.TISSUE SPECIFICITY: Brain and testis.DISEASE: SwissProt: P15056 # Defects in BRAF are a cause of cardiofaciocutaneous syndrome (CFC syndrome) [MIM:115150]; also known as cardio-facio- cutaneous syndrome. CFC syndrome is characterized by a distinctive facial appearance, heart defects and mental retardation. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. The inheritance of CFC syndrome is autosomal dominant. & Defects in BRAF are involved in a wide range of cancers. & Defects in BRAF are involved in lung cancer [MIM:211980]. & Defects in BRAF are involved in non-Hodgkin lymphoma (NHL) [MIM:605027]. NHL is a cancer that starts in cells of the lymph system, which is part of the body's immune system. NHLs can occur at any age and are often marked by enlarged lymph nodes, fever and weight loss. & Defects in BRAF may be a cause of colorectal cancer (CRC) [MIM:114500].SIMILARITY: SwissProt: P15056 ## Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family. RAF subfamily. & Contains 1 phorbol-ester/DAG-type zinc finger. & Contains 1 protein kinase domain. & Contains 1 RBD (Ras-binding) domain. View All» Species: Human View All» Molecular Weight: 67.2kDa View All» Brand Family: Upstate View All» Source: Expressed by baculovirus in Sf21 insect cells View All» Protein Target: B-Raf View All» Storage Conditions: 6 months at -70°C View All» Target Sub-Family: TKL View All» Gene Symbol:

• BRAF

• BRAF1

• B-Raf

• MGC126806

• RAFB1

• p94

• MGC138284

• B-raf-1
  View All» Product Name: B-Raf (δ1-415), active View All» Quality Assurance: routinely evaluated by phosphorylation of MBP substrate in vitro View All» UniProt Number: P15056 View All» Specific Activity: For Specific Activity data, refer to the Certificate of Analysis for individual lots of this enzyme. View All» Packaging: Also available in 10 μg size (cat#14-530) and in bulk (cat# 14-530-K). View All» Entrez Gene Number: NM_004333.3 View All» Purification Method: Glutathione agarose affinity chromatography View All»
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