rongsheng mobile bd private ltd supplier

Rongsheng Mobile India Private Limited is an Indian private company incorporated on 24/11/2014 and its registered office address is 503, Royal Centre, 5th Floor, GS Road,Opp. SB Deora College, Bora Service,Guwahati,Assam,INDIA,781007. The company"s Annual General Meeting (AGM) was last held on 2015-09-30 and its balance sheet was last filed on 2015-03-31. The current age of the company as per its registration date is 8 Years 2 Months 12 Days and is classified as the Indian Non-Government Company.

Rongsheng Mobile India Private Limited is registered at Registrar of Companies, Shillong (RoC-Shillong). Bin Luo is the director of this company. in the year 2014.2014-11-24The company has 1 director on the board at the time of inception and was appointed on the date 2014-11-24. The contact details of the company are mentioned in the contact section or you could contact them by submitting the request for quote form on their website.

Rongsheng Mobile India Private Limited is a retailer company with the National Industrial Classification (NIC) code of 52392. Based on this activity code, the company is involved in the business activities such as Computers and non-customized software, retail sale by specialized stores,#Retail sale of computers and non-customized software#.

shin rong sheng enterprises co.ltd. is a Taiwan Supplier, the following trade report data is derived from its trade data; the company"s import data up to 2022-09-23 total 230 transactions. Based on these trade data, we have aggregated the data in terms of trading partners, import and export ports, countries of supply, HS codes, contact details and other dimensions, which will help you to improve the efficiency of using your foreign trade data.

The graph above shows the market trend analysis of shin rong sheng enterprises co.ltd. for the past year, which can be used to understand the current supply cycle and business stability of the company from the trend of different dimensions such as quantity, weight, price and number of transactions.

shin rong sheng enterprises co.ltd. is A Taiwan Supplier. This Company"s Trade Report Mainly Contains Market Analysis, Contact, Trade Partners, Ports Statistics, And Trade Area Analysis. Official Reference Contact Is From Taiwan Original Bill Of Ladings, Including Email, Phone, Fax, Address, And Official Website. Till 2022-09-23，shin rong sheng enterprises co.ltd.. A Total Of 230 Transactions. Follow Up The Company, And Then Can Export This Company"s Contact And B/Ls. If There Is New Transactions, We Will Also Inform You By The System.

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SHANGHAI, Oct 30 (Reuters) - China Rongsheng, the country’s largest private shipbuilder, has secured a cash lifeline that could be worth up to HK$3.23 billion dollars and is looking to change its name to reflect its shift into oil exploration.

Shares in heavily indebted Rongsheng, which were suspended on Aug. 29 after the company said it was in the process of restructuring, surged almost 17 percent higher after trading resumed on Thursday. They reversed gains, and were down 3.7 pct by 0217 GMT.

Rongsheng said late on Wednesday it would issue warrants worth HK$510 million to a Cayman Islands-incorporated investment firm wholly owned by private equity investor Wang Ping, which would entitle subscribers to buy up to 1.7 billion new shares at HK$1.60 each.

This would raise about HK$3.23 billion for Rongsheng, it said. A warrant entitles the holder to buy stock from the issuer at a specific price within a time frame.

The price of the new shares is at a 17.65 percent premium to Rongsheng’s closing price of HK$1.36 per share on Aug. 28, when it last previously traded. It said the subscription shares represent 19.36 percent of the firm’s issued share capital.

Rongsheng, which builds Brazilian miner’s Vale mega-iron ore carriers, came close to insolvency last year before clinching an agreement with banks to extend its loans until end-2015.

As one of the Jiangsu region’s largest employers, the firm has received copious support from the government, which is currently helping Rongsheng with its restructuring.

Rongsheng also said it had signed a debt agreement with a syndicate of domestic banks in Anhui province that would extend its debt payments to the end of 2015.

Rongsheng has been one of the most prolific casualties of the global shipping slump. The industry is still trying to shake off a glut of ships ordered before the crisis which has sunk freight rates and caused many shipbuilding orders to be delayed or cancelled. ($1 = 7.7552 Hong Kong dollar) ($1 = 6.1136 Chinese yuan) (Reporting by Brenda Goh; Editing by Miral Fahmy)

Rongsheng Mobile India Private Limited is a Non-govt company, incorporated on 24 Nov, 2014. It"s a private unlisted company and is classified as"company limited by shares".

Company"s authorized capital stands at Rs 500.0 lakhs and has 51.0% paid-up capital which is Rs 255.0 lakhs. Rongsheng Mobile India Private Limited last annual general meet (AGM) happened on 30 Sep, 2017. The company last updated its financials on 31 Mar, 2017 as per Ministry of Corporate Affairs (MCA).

Rongsheng Mobile India Private Limited is majorly in Trading business from last 9 years and currently, company operations are active. Current board members & directors are ZHAORONG LI, XIAOBIN ZHENG, ZHAOHUI LI, TAO XIE, HAIPING LI, HAOFEI YAN, TAO YANG, XINGJUN XIAO, XIANGWEN XIAO and YAQING DUAN .

Company is registered in Shillong (Assam) Registrar Office. Rongsheng Mobile India Private Limited registered address is 7TH FLOOR, DEE TEE TOWERS DOWN TOWN HOSPITAL COMPLEX, G.S ROAD , DISPUR GUWAHATI Kamrup AS 781006 IN.

Lenze Drive Systems (Shanghai) Co., Ltd. is the local representation of the Lenze group in the People"s Republic of China. With our production plant and logistics center in Shanghai Lingang Heavy Equipment Zone and our 11 sales offices throughout China, we are able to provide the complete Lenze product portfolio - from the control system to the drive shaft!

For adoptive transfer (AT) experiments, donor mice were immunized with tAChR (20µg of tAChR/CFA in 100 µl subcutaneously followed by one booster at 24–30 days later (day 0) and treatment with GM-CSF (2 µg daily IP for 10 days) or PBS. These donor mice were sacrificed 14 days after GM-CSF treatments (24 days after the booster immunization). Splenic CD19+ B cells were isolated from mice by positive selection using magnetic beads (Miltenyi Biotec, Auburn, CA) with obtained purity ≥ 95%. CD1dhiCD5+ and CD1dloCD5− B cells were purified (95–98%) using a FACSAria flow cytometer (BD Biosciences). After purification, CD1dhiCD5+ B cells (1 × 106) were immediately transferred into appropriate recipient mice by tail vein injection.

Single cell suspensions of splenocytes were prepared from mice sacrificed upon the completion of the GM-CSF/PBS treatment regimen for flow cytometric analysis. Cells were washed with PBS supplemented with 0.05% BSA, blocked with antiCD16/CD32 Fc-Block (BD PharMingen, San Jose, CA) on ice for 30 min. APC-conjugated anti-CD19, PB-conjugated anti-CD5 and PE-conjugated anti-CD1d (BioLegend), anti-IAb (MHC class II), anti-CD40, anti-CD80, anti-CD86, isotype control antibodies (Abs) (BD PharMingen) were used in flow cytometry and analyzed using FlowJo software (Treestar, Ashland, OR). Mouse regulatory T cell staining kit (w/ PE FoxP3 FJK-16s, FITC CD4, APC CD25 Abs) (eBioscience) was used for intracellular staining for FoxP3 expression. PE-conjugated antibodies against IL-10, IL-17A, and IFN-γ were used for intracellular cytokine staining of T or B cells. For B10 cells, isolated leukocytes or purified cells were resuspended (2 × 106 cells/ml) in complete medium (RPMI 1640 containing 10% FCS, 200 µg/ml penicillin, 200 U/ml streptomycin, 4 mM L-glutamine, and 5 × 10−5 M 2-ME; all from Invitrogen, Carlsbad, CA, USA) in the presence of lipopolysaccharide (LPS) (10 µg/ml; Sigma, St. Louis, MO, USA), phorbol 12-myristate 13 acetate (PMA) (50 ng/ml; BD PharMingen), ionomycin (500 ng/ml; BD PharMingen), and monensin (2 µM; BD PharMingen) in 48-well, flat-bottom plates for 5 h at 37 °C. Cells were fixed and permeabilized using the Cytofix/Cytoperm kit. Permeabilized cells were stained with PE-conjugated anti-IL10 antibody. For intracellular T cell cytokine analysis, the same protocol was used except LPS was omitted.

Splenic CD1dhiCD5+ B cells from donor mice in the PBS/EAMG (AChR-immunized mice receiving PBS) and in the GM-CSF/EAMG (AChR immunized mice receiving GM-CSF) groups were isolated and co-cultured with responder T or B cells from immunized mice at 1:1 ratio. For proliferation assay, responder CD4+ or CD19+cells were isolated from mice in untreated EAMG mice using magnetic cell sorting (Miltenyi Biotec, Auburn, CA) and were stained with CFSE at a concentration of 1 µM for 10 min at 37 oC. Cells were washed three times and plated into 96-well, flat-bottom plates at 5 × 105 cells/well. T cell-depleted enriched DCs (1 × 105 cells/well) (also accomplished by magnetic cell sorting) were used as feeder cells in these studies. Cells were stimulated with tAChR (5 µg/ml) for 72 hrs, and then harvested for CFSE dilution studies and intracellular cytokine expression using a FACS analyzer (BD Biosciences). For antibody production, total anti-AChR IgG concentrations in culture supernatants in B cell co-cultures were measured using a mouse IgG enzyme-linked immunosorbent assay (ELISA) set (Bethyl Laboratories, Montgomery, TX), according to the manufacturer’s specifications.