Subtotal:
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FastCellular senescence detection kit – SPiDER-?Gal, 1 kit
₹100.00The FastCellular senescence detection kit provides:
Higher sensitivity due to a new fluorogenic detection probe
Applicable for living cells and fixed tissues
Ability to quantify SA-?-gal in cellular senescence assay
Short staining time (30 min) -
FastGro Synthetic, Animal Free, Chemically Defined FBS Replacement
₹100.00FastGro is a fully define medium that allows culturing cells in vitro without the use of serum and without any animal or human derived compound.
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FastMitophagy detection kit, 1 kit
₹100.00The FastMitophagy Detection Kit is specifically designed for mitophagy detection in mammalian cells.
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Gellan gum powder
₹100.00Gelrite, gellan gum, is recommended as a gelling agent for use in place of agar in microbiological media.
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GS96 medium, powder
₹100.00GS96 broth delivers high yields of plasmid DNA in 96-well and 384-well plates
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Ham’s F-10 (10X) w/o L-glutamine, w/o sodium bicarbonate, with 12.4 mg/L phenol red, 100 mL
₹100.00Hams F10 medium is a nutrient mixture designed to cultivate a wide variety of mammalian and hybridoma cells.
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Ham’s F-10, with L-glutamine, w/o sodium bicarbonate, powder for 10 L
₹100.00Hams F10 medium is a nutrient mixture designed to cultivate a wide variety of mammalian and hybridoma cells.
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Ham’s F-12 (modified) wih L-glutamine, w/o sodium bicarbonate
₹100.00Ham’s F-12 medium was designed for low density, serum-free growth of Chinese Hamster Ovary (CHO) cells. Ham’s F-12 is well suited for the growth of primary rat hepatocytes and prostate epithelial cells. It is also the medium of choice for toxicity assays using CHO cells.
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Ham’s F12 (1X) with L-glutamine, 500 mL
₹100.00Ham’s F-12 medium was designed for low density, serum-free growth of Chinese Hamster Ovary (CHO) cells. Ham’s F-12 is well suited for the growth of primary rat hepatocytes and prostate epithelial cells. It is also the medium of choice for toxicity assays using CHO cells.
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Hank’s Balanced Salts (Hbs) (modified) (1X) w/o Ca, Mg, phenol red, 500 mL
₹100.00Hank’s Balanced Salts (HBS) (Modified) (1X Solution) without calcium, magnesium, phenol red
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Hanks’ Balanced Salts, powder, w/o sodium bicarbonate
₹100.00Hanks’ Balanced Salts solution is used to maintain the pH and osmotic balance in the medium and to provide the cells with water and essential inorganic ions.
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Hat supplement (50X solution), 100 mL
₹100.00Selective for hybridoma cell growth and growth of cells with a functioning HGPRT mechanism. The main application is for the selective growth of hybridoma cells for monoclonal antibody production. (50x formulation: 13.61 mg/L hypoxanthine, 0.1906 mg/L aminopterin 2H2O,3.876 mg/L thymidine.)
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Hemoglobin, 500 g
₹100.00Hemoglobin, from beef blood. Autoclavable preparation to be used with GC Agar Base.
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HEPES buffer, cell culture grade, 20 g
₹100.00Cell culture grade HEPES (powder). Buffer strength for cell culture applications is usually in the range of 10 to 25 mM. Studies have indicated that 20 mM HEPES is the most satisfactory concentration of the buffer when both Hanks’ and Earle’s solutions are used.
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High Growth Enhancement Medium (GEM), (1X) w/o L-glutamine, 500 mL
₹100.00High Growth Enhancement Medium, without L-Glutamine is a modification of DMEM in which 3.6 g/liter fructose is substituted for glucose, resulting in better pH control and higher cell yields. Fructose is metabolized slower than glucose, resulting in slower acid buildup.
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High Growth Enhancement Medium (GEM), with L-glutamine, w/o sodium bicarbonate, 10 L
₹100.00High Growth Enhancement Medium is a modification of DMEM in which 3.6 g/liter fructose is substituted for glucose, resulting in better pH control and higher cell yields. Fructose is metabolized slower than glucose, resulting in slower acid buildup.
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HL5 medium, 454 g
₹100.00HL5 Medium supports the growth of Dictyostelium discoideum strains capable of growing axenically (without bacteria as food.)
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Hoagland’s modified basal salt mixture
₹100.00Hoagland’s Modified Basal Salt Mixture includes the macro- and micronutrients as described by Hoagland and Arnon, 1950.
