Reliable Newborn Screening devices provided by Labsystems Diagnostics.
OVERVIEW
Stand-alone NS96 Disc Remover effectively removes the sample discs after incubation and reduces the chances of cross-contamination
No products in the cart.
MPIN: MP41169
Sign in to view priceReliable Newborn Screening devices provided by Labsystems Diagnostics.
Reliable Newborn Screening devices provided by Labsystems Diagnostics.
OVERVIEW
Stand-alone NS96 Disc Remover effectively removes the sample discs after incubation and reduces the chances of cross-contamination
Orders made at Medpick are initiated and processed for shipment upon receipt of request from the customer. Please note that our Shipping Services (Fee, Transportation, Loss or Damage of any shipment, etc.) are in accordance with the Seller\'s terms of Shipment.
Please refer to Medpick Return Policy.
Please refer to Medpick Return Policy.
Congenital hypothyroidism (CH) is an endocrine disorder of newborns characterized by the decreased levels of thyroid hormones: thyroxine (T4) and triiodothyronine (T3) in periferal blood. In early perinatal period manifestations of CH are often non-specific, subtle or even non-existent [1-2]. However, the disease, if undiagnosed and untreated, leads to severe
Congenital Adrenal Hyperplasia (CAH) includes a group of disorders in which the cortisol production by adrenals is lowered. Cortisol is a steroid hormone necessary to maintenance of blood sugar level, partial maintenance of body fluids and electrolytes and protection of the body against stress. CAH cannot be cured, but it can be effectively treated by steroid substitution therapy if detected in early stage of life and disease course.
Say Goodnight to Overnight tissue processing The Tissue-Tek® Xpress® x120 Continuous Rapid Tissue Processor is a self-contained tissue processor employing microwave and vacuum infiltration techniques. The instrument performs automatic rapid processing (fixation, dehydration, clearing, and paraffin impregnation) of tissue specimens in preparation for histological study and examination.
Galactosemia is an inherited metabolic abnormality comprising three distinctive clinical entities of the galactose pathway defects. Classic galactosemia is due to -Dgalactose- 1-phosphate-uridyl-transferase (GALT) defect (1). The test principle is based on extraction of Galactose & Galactose-1-phosphate from dried blood spot followed by enzymatic conversion of Galactose-1-phosphate & Galactose. Two kinds of extraction methods (acidic and heat) can be used for extraction step.
Sign up for Insider Pricing and get access to attractive discounted prices on commercially rated products as well as dedicated Account Representatives to manage your orders.
Sign up for Insider Pricing and get access to attractive discounted prices on commercially rated products as well as dedicated Account Representatives to manage your orders.