Gene:  AMMECR1, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair gene expression assay target

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The exact function of this gene is not known however submicroscopic deletion of the X chromosome including this gene COL4A5 and FACL4 genes result in a contiguous gene deletion syndrome the AMME complex (Alport syndrome mental retardation midface hypoplasia and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq Jan 2010]

PrimePCR™ SYBR® Green Assay: AMMECR1, Human
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0042890
Info:   Same primer pair as used in probe assay qHsaCEP0050152
List Price:    $146.00
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PrimePCR™ SYBR® Green Assay: AMMECR1, Human
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1

Assay Type: SYBR® Green
Assay Design: Intron-spanning
Application: Gene Expression
Unique Assay ID: qHsaCID0006462
Info:   Recommended - best efficiency
List Price:    $146.00
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PrimePCR™ Probe Assay: AMMECR1, Human
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0050152
List Price:    $214.00
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    Related pathways not available
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