RN46A

NOTE: Both the cell line and DNA from the cell line may be available for this product. Please choose -1VL or VIAL for cells, or -DNA-5UG for DNA, 12061302, rat embryo d13 medullary raphe. Morphology: proliferating, fibroblast. Differentiating, neuronal.

• 分類程式碼代碼: 41106514

屬性

• 生物源: rat embryo (day 13 medullary raphe)
• 包裝: tube of 5 μg 12061302-DNA-5UG; pkg of vial of cells 12061302-1VL
• 增長模式: Adherent
• 染色體組型: Not specified
• 形態學: Fibroblast morphology while proliferating and neuronal on differentiation
• 受體: Not specified

描述

細胞系來源

Embryonic rat medullary raphe, temperature-sensitive mutant of SV40 large T-antigen, immortalised, serotonergic, neuronal

細胞系描述

RN46A , an immortalized serotonergic neuronal cell line, was cloned by serial dilution following infection of dissociated embryonic day 13 rat medullary raphe cells with a retrovirus encoding the temperature-sensitive mutant of SV40 large T-antigen (T-ag), RN46A cells are capable of differentiating at 39 °C the non-permissive temperature. Under differentiation conditions, RN46A cells cease dividing, take on a neuronal morphology, and express enhanced levels of NSE and all three NF proteins. Differentiated RN46A cells express low-affinity nerve growth factor (NGF) receptor (p75NGFR) and are i mMunoreactive using an antibody that recognizes the carboxy-terminal 13 amino acids of all three trk proteins (pan-trk). Both i mMunoreactivities could be potentiated by treatment with brain-derived neurotrophic factor (BDNF), NGF, and adrenocorticotropic hormone, fragment 4-10 (ACTH4-10). Differentiated RN46A cells express low levels of tryptophan hydroxylase (TPH) i mMunoreactivity, which could be enhanced by treatment with ACTH4-10, BDNF, or NGF. Low levels of serotonin i mMunoreactivity are detected in differentiated RN46A cells, and this was potentiated by differentiating RN46A cells with BDNF for 8 d and 40 mM KCl for days 4-8. RN46A cells should prove useful to elucidate intracellular mechanisms that control neurofilament assembly and 5-HT expression in differentiating raphe neurons.

DNA分析

Not specified

培養基

DMEM:F12 (1:1) (D8062) + L-Glutamine (G7513) + 10% FBS / FCS (F2442) + 0.25mg/ml Geneticin (G418). Alternatively CNS medium can be used (see Kawamoto & Barrett 1986). Differentiation can be induced as follows: cells growing at 33 °C are sub-cultured onto collagen/fibronectin matrix (100 μg/cm² air-dried collagen I from rat tail followed by 1 μg/cm² fibronectin). Sub-confluent cells (75%) are shifted to 39 °C. The culture medium is changed to DMEM:F12 (1:1) (D8062) + 1%(w/v) bovine serum albumin (BSA) + 1 μg/ml bovine transferrin + 5 μg/ml bovine insulin + 100 nM putrescine + 20 nM progesterone.

例行更新培養

Split subconfluent cultures (70-80%) 1:2 to 1:5 using 0.25% trypsin/EDTA; 5% CO₂; 33 °C. Suggested seeding density 2-4 x 10,000 cells/cm². Doubling time 19hrs.

其他說明

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