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(+91)-120-3634639Immunofluorescence Assay (IFA) is a powerful technique used to detect specific proteins or antigens within cells or tissues using antibodies conjugated to fluorescent dyes. This method is widely used in cell biology, pathology, and diagnostics for studying cellular structures, protein localization, and disease markers..
- Karyotyping Analysis
- Fluorescence In-Situ Hybridization (FISH)
- Molecular Genetics Services
- Chromosomal Microarray Analysis (CMAn
Karyotyping is the process
of viewing chromosomes under a microscope during the
metaphase phase of cell division and organizing them
into a karyogram using a standard format that
includes banding patterns, size, and shape.
- Chromosomal Abnormalities
- Prenatal
Testing
- Infertility and Miscarriage Analysis
- Cancer Diagnosis
- Reproductive Medicine.
A molecular cytogenetic approach called Fluorescence In Situ Hybridization (FISH) locates and identifies particular DNA sequences on chromosomes or inside cells using fluorescent probes. Because of its accuracy and capacity to identify particular genetic disorders, this method is frequently used in clinical diagnostics, genetic research, and oncology.
A variety of laboratory
methods for molecular analysis of DNA, RNA, and
genetic variants are included in molecular genetics
services. These services are essential for
determining disease predispositions, detecting
genetic illnesses, directing personalized care, and
assisting with genomics research.
- DNA &
RNA Sequencing
- Analysis by Real Time PCR
-
Mutation and Variant Analysis
- DNA Methylation
Analysis
- Genetic Disease Testing
- Cancer
Genetics.
A high-resolution method for identifying chromosomal abnormalities including copy number variations (CNVs) and homozygosity regions throughout the genome is called chromosomal microarray analysis, or CMA. In clinical diagnostics for genetic abnormalities, it is a commonly utilized tool, especially in cancer, pediatric, and prenatal diagnoses..
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