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PCR芯片
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SABio
| Product | Species | Technology | Cat. No. |
| Cell Lineage Identification PCR Array | Human | Gene Expression | PAHS-508Z |
| Cell Lineage Identification PCR Array | Mouse | Gene Expression | PAMM-508Z |
| Cell Lineage Identification PCR Array | Rat | Gene Expression | PARN-508Z |
Pluripotent Markers: DNMT3B, GDF3 (VGR-2), LEFTY1, NANOG, PODXL, POU5F1 (OCT4), ZFP42. Germ Layers: Ectoderm: FGF5, FOXD3, OTX2, ZIC1. Neuroectoderm: GBX2, NEUROG2. Mesoderm: BMP4, CD34, DCN, GATA2, HAND1, IGF2, MIXL1, PDGFRA, RUNX1 (AML1), T (Brachyury). Endoderm: FOXA1, GATA1, GATA6, HNF4A, SOX17, SOX7. Progenitors: Ectoderm: Neuronal: FABP7, HES5, PROM1, SOX2. Immature Neuron: DCX. Immature GABA Neuron: GAD2, SLC32A1. Limbal Progenitor: ENO1, MSLN. Motor Neuron Progenitor: FOXG1, OLIG2. Oligodendrocyte Progenitor: NKX2-2, OLIG2. Mesoderm: Early Cardiomyocyte: HAND2. Early B Cell: CD79A. Early T Cell: CD3E, PTCRA. Muscle Stem Cell: CD34. Endoderm: Pancreatic Islet Cell: KRT19. Hepatic Stem Cell: APOH, DPP4, MAP3K12. Terminal Differentiation: Ectoderm: Keratinocyte: KRT10, KRT14. Melanocyte: TYR. Mature Neuron: NEUROD1. Cholinergic Neuron: CHAT. GABA Neuron: GAD1. Glutamatergic Neuron: SLC17A6, SLC17A7. Astrocyte: GALC, GFAP. Ganglion Cell: POU4F2. Photoreceptor Cell: RCVRN. Mesoderm: Skeletal Muscle Cell: MYH1. Smooth Muscle Cell: MYH11, SMTN. Cardiomyocyte: MYL3, MYH7, NPPA, RYR2. Osteoblast: IBSP. Osteoclast: CTSK. Chondrocyte: COL10A1, COMP. Macrophage: CCR5. Endoderm: Hepatocyte: ALB, G6PC, TAT. Cholangiocyte: ITGB4. Beta Cell: INS, SLC2A2. Exocrine Cell: CPA1. Lung Cell: SFTPB, SFTPD. Proximal Tubule Cell: AQP1, MIOX.
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文献和实验Lineage Analysis of Inner Ear Cells Using Genomic Tags for Clonal Identification
To understand the mechanisms of development of the inner ear, it is important to know the lineal relationships among the different cell types and the migrational boundaries of individual clones within the inner ear. This chapter details the basic
genes. In this approach, a multiplex polymerase chain reaction (PCR) incorporating digoxigenin-dUTP is used to simultaneously amplify different marker genes, with subsequent rapid detection of the amplicons by hybridization with an array of probes
Complete Array of HOX Gene Expression by RQ-PCR
or some of their regulatory factors, e.g., mixed lineage leukaemia (MLL), leading to inappropriate expression of certain subsets of the genes. Evolutionarily, the HOX genes are thought to have arisen by duplication and divergence from a primordial gene. Consequently
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