Laboratory：Hachioji
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- Dystrophin gene analysis (Duchenne muscular dystrophy Becker muscular dystrophy)
Laboratory：Hachioji
○Dystrophin gene analysis (Duchenne muscular dystrophy Becker muscular dystrophy)
CODE：6236 9
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TEST NAME
SPECIMEN
REQUIREMENT
（ｍL） CONTAINER CAP COLOR STORE
TEMPERATURE
(STABILITY) TURNAROUND
TIME (DAY) METHODOLOGY REFERENCE RANGE
(UNIT) -
Dystrophin gene analysis (Duchenne muscular dystrophy Becker muscular dystrophy)
Blood (EDTA-2Na added)
7
PN7
12-16 MLPANo gene deletions or duplications observedMLPA (Multiplex ligation-dependent probe amplification)
After hybridizing a specific probe fused with a common PCR primer sequence to the labeled region, PCR is performed, and quantitative changes in the amplified products are investigated using a relatively large genome. Methods for detecting deletions or duplications.
COMMENT
Avoid freezing. All 79 regions of the dystrophin gene will be analyzed for deletion and duplication mutations. Please note that we cannot analyze DMD gene mutations other than exon deletions and duplications, including minute deletions, duplications and insertions, single nucleotide substitutions, and splice mutations. Additionally, if a mutation is detected only in a single exon, it may be a mismatched sequence such as a single nucleotide substitution. This testing method increases the influence of contamination, so please be careful when handling the specimen.
Ethical guidelines (see below)
Collect blood into the container shown below, mix well, and store in the refrigerator.
This testing method increases the influence of contamination, so please be careful when handling the specimen.
CONTAINER
PN7 旧容器記号 A 4
EDTA-2Na入り (真空採血量7mL)
内容：EDTA-2Na 10.5mg
貯蔵方法：室温
有効期間：製造から2年
