Lan-Ao

AutoPlex-12,AutoPlex-Mini,and Detection Kits

• Easy to Use

  ntegrating functions such as sample nucleic acid extraction, amplification detection, and analysis, from input to output.
  Using pre-packaged reagents, one-click software operation enables full automation of nucleic acid detection experiments.

• Testing Process

  Sample types: whole blood, serum, plasma, nasal/oropharyngeal swabs, feces, bronchoalveolar lavage fluid, cerebrospinal fluid, etc.
  One run can detect 1-12 samples, with each sample being able to test up to 16 targets simultaneously.
  The entire process takes less than 1.5 hours.

• Core Strengths

  The platform is fully open and utilizes universal consumables (0.2mL PCR eight-tube strip), compatible with most commercially available fluorescent PCR/PCR fluorescent probe nucleic acid detection reagents from various manufacturers.
  The performance of nucleic acid extraction or purification reagents is stable.
  Using single-strip and single-person pre-packaged reagents, the operation is flexible and convenient.

• Application: Human leukocyte antigen B27 gene detection(The detection kit can privede)

  Ankylosing spondylitis (AS) is a chronic inflammatory disease with an insidious onset and slow progression, posing a high risk of disability. HLA-B27 gene testing holds significant importance in the early screening and diagnosis of AS, as well as in seizing the optimal opportunity for treatment.

• Application: Human MTHFR gene polymorphism detection(The detection kit can privede)

  MTHFR, or Methylenetetrahydrofolate Reductase, is a crucial enzyme in the human folate (vitamin B9) metabolic pathway, playing a central role in maintaining normal physiological functions. The C677T gene mutation is the most widely studied and clearly health-related functional variation in the MTHFR gene. Its core impact is to alter the activity of the MTHFR enzyme, thereby significantly affecting the efficiency of human folate metabolism and homocysteine levels, which can lead to conditions such as neural tube defects, Down's syndrome (congenital idiocy), cleft lip and palate, congenital heart disease, pregnancy-induced hypertension, premature birth, and preeclampsia.