Step 1: In hybridoma technology, myeloma cells are fused with B-cells to produce hybrid cells capable of indefinite growth and antibody production.
Step 2: Myeloma cells used in this process are deliberately deficient in the enzyme Hypoxanthine-guanine phosphoribosyltransferase (HGPRT).
Step 3: This allows for the selection of hybridoma cells in HAT medium, because unfused myeloma cells die (due to HGPRT deficiency) and unfused B-cells die naturally as they cannot grow indefinitely.
Step 4: Only fused hybridomas survive and proliferate. Hence the absent enzyme is HGPRT.