cscbtissuelab@gmail.com
04931 231252, 231253, 230253

We provide tissue cultured plants and also offers modern fertilizers as per demand. Check out more information below.

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Banana Tree Tissue Culture

Highlights

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Quality seedlings

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Disease free seedlings

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Production of excess seedlings in a short period of time

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Uniformity in growth and yield

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Seedling production as per-determined

How to care Banana Tree Tissue Culture plant

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Handle the seedlings carefully.

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Seedlings should be 15 to 20 cm long and have at least four leaves.

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Good drainage is essential and avoid waterlogged areas.

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Acidity: 6.0-7.5

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Pit size:50x50x50cm

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Compost / Dung: 10kg

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Cut the polythene cover and plant the planting mixture without disturbing the seedlings.

Fertilizer application

Sl. No Time for applying Fertilizer Urea (Grm) Masuri Fos Raj Fos (Grm) Muriate of Potash (Grm)
1 One month after planting 110 360 110
2 Two months after planting 110 110
3 Three months after planting 110 280 110
4 Four months after planting 110 110
5 Five months after planting 110 110
6 After the bunch of bananas came 110 215

The trace elements zinc, iron, boron and copper manganese are also crucial for the growth of tissue culture bananas. In the absence of these, the growth of the banana is completely inhibited and some symptoms are manifested.

Resources containing the above mentioned trace elements can be used in the third and fifth months.

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Ornamental Plants Tissue Culture

ORCHIDS

The cultivation of monocot explants is more difficult to culture than dicot explants. However, some parts of some species of orchids, like floral meristem and protocorms of genus Cymbidium, can be cultured using a simple vitamin B-containing medium.

Requirements

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Rimless culture tubes containing 10 ml agar medium.

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Tissue paper

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Erlenmeyer flasks (250 ml) containing 200 ml distilled water.

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Petri dishes

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Aluminum foil

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Forceps

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Scalpels

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Pseudobulbs of Orchids

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Glass beaker containing 200 ml 20% solution (v/v) of a commercial bleach preparation.

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Glass beaker (250 ml) containing 200 ml of 95% ethanol.

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Metal scalpel

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Bunsen burner

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Erlenmeyer flask containing 100 ml 95% ethanol.

Procedure

  • Take the pseudobulbs and remove all the side buds, revealing meristem.
  • The meristem will still be covered with the small leaves.
  • Cut through the base of buds with a scalpel and dip the pieces in the 95 % ethanol for 10 seconds.
  • Take out the buds and remove the extra ethanol and then immerse the pieces again in the hypochlorite solution for 25 minutes.
  • Remove the buds from the solution and wash them thoroughly with three changes of sterile distilled water.
  • Place buds in the 95 % ethanol for 10 seconds to remove the leaves.
  • After removing leaves, rinse the explant with sterile water.
  • Carefully separate the meristem using a sharp scalpel under a microscope.
  • Place the meristem in agar-containing cultured tubes.
  • Incubate the culture in white light at 25 ℃ for 8 days.
  • After 8 days, a perfect green-colored protocorm will be visible.
  • Subdivide the protocorm in the cultured tubes using a sharp sterile scalpel.
  • Place the pieces on agar, flame the mouth of the tube, and cover it using aluminum foil.
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Advanced Fertilizing Techniques

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Production of Tissue culture Plants in rare and extinction crop sps.

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Production of Bio-manures.

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Production of Bio-fertilizers and Bio-pesticides.

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Corporate Farming (Organic Farming).

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Shared Farming.

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Turnkey Projects.

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Contract Production.

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Design and implementation of Plant tissue culture Labs & Green House Facilities.

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Research and Training in emerging fields of Biotechnology.

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