PrimePCR™ Probe Assay: BCL2L1, Human

RT

Real-time PCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

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PrimePCR™ PreAmp for Probe Assay: BCL2L1, Human
Reaction:     400 reactions
Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for subsequent use in downstream gene expression analysis.

PrimePCR™ Template for Probe Assay: BCL2L1, Human
Reaction:     200 x 20 µl reactions
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding probe assay.


Wet Lab Validated

Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0039517
Assay Design:   exonic
Chromosome Location:   20:30309967-30310109question
Amplicon Length:   113
Splice Variants Targeted:   ENST00000376062 ENST00000376055 ENST00000307677 ENST00000450273 ENST00000422920 ENST00000456404 ENST00000420488 ENST00000439267 ENST00000434194 ENST00000420653

Gene Information

The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The proteins encoded by this gene are located at the outer mitochondrial membrane and have been shown to regulate outer mitochondrial membrane channel (VDAC) opening. VDAC regulates mitochondrial membrane potential and thus controls the production of reactive oxygen species and release of cytochrome C by mitochondria both of which are the potent inducers of cell apoptosis. Two alternatively spliced transcript variants which encode distinct isoforms have been reported. The longer isoform acts as an apoptotic inhibitor and the shorter form acts as an apoptotic activator. [provided by RefSeq Jul 2008]

Gene Symbol:   BCL2L1
Gene Name:   BCL2-like 1
Aliases:   BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, DKFZp781P2092, bcl-xL, bcl-xS
RefSeq:   NC_000020.10 NT_011362.10
Ensembl:   ENSG00000171552
Entrez:   598
Chromosome Mapping:   20q11.21

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