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Beta Thalassemia Dna Based Mutation Study
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Beta Thalassemia Dna Based Mutation Study

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Beta Thalassemia is a type of autosomal recessive disease. Maternal and paternal mutations comes inheritance into child. If the both beta globulin chain gene are defected, it result into thalassemia major. So, its very importance to detect genetic mutation of parents/couple who are thalassemia minor, when they are planning for baby. It is possible to diagnose prenatally and...
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Shree Krushna Gene Lab & Research Center

Manohar Plot, Rajkot, Gujarat
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Beta Thalassemia is a type of autosomal recessive disease. Maternal and paternal mutations comes inheritance into child. If the both beta globulin chain gene are defected, it result into thalassemia major. So, its very importance to detect genetic mutation of parents/couple who are thalassemia minor, when they are planning for baby. It is possible to diagnose prenatally and can manage according. Expert doctors and scientist do this job to cater good service.

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Beta Thalassemia Dna Based Mutation Study

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About us

Nature of BusinessService Provider
IndiaMART Member SinceOct 2014

Introduction:

Shree Krushna Gene Lab and Research Centre supports genetic diagnosis and research on the human and model genomes and on all aspects of genetics, basic biochemistry and cell biology related to health and disease, including the translation of knowledge into health policy and practice, and the societal implications of genetic discoveries.

Infrastructure:

Shree Krushna Gene Lab and Research Centre design for Cytogenetic and molecular genetic diagnosis cum research full pledge laboratory. Each test is tested by trained and experienced technicians under the supervision of qualified Scientist.

Diagnostic services:

  1. Chromosome Karyotyping services from: Blood, Bonemarrow, Amniotic fluid, Cancer Cells, tissue, Asiatic fluid, Product of conception (POC)
  2. Molecular diagnosis tests (PCR BASED): TB, HIV, MTB, beta thalassemia, Y chromosome micro deletion, HLA B27, Cystic fibrosis, etc..

Predictive Toxicology Testing:

Toxicology profile with range in primary profiling and complete profiling of any novel, synthetic and analogue compound of commercial, pharmaceutical, industrial or any part of health sector are served according to need. (OECD guideline ) The wide range allows selective or complete profile study of compound depending upon the purpose of use and application. The few services under this portfolio are:

1. In Vitro Toxicity assay 2. In Vitro Geno Toxicity assay 3. Molecular Genotoxicity assay 4. Environmental toxicity 5. Drug/ Chemical / Dye genotoxicity 6. Cancer genetics

OECD 473 : “In Vitro Mammalian Chromosome Aberration Test”

OECD 479 : “Genetic Toxicology: In vitro Sister Chromatid Exchange

Assay in Mammalian Cells”

OECD 487 : “In Vitro Micronucleus Test”

OECD/Guideline : “COMET assay – Single cell electrophoresis”

OECD/Guideline : “MTT assay” Cell Viability testing.

OECD/Guideline : “Trypan blue” Cell Viability testing.

OECD 471 : “AMES Test – Bacterial Reverse Mutation Test”

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