| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| APOA2-ITPR2-20-RERE | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-REOR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-REGO | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-REGR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-REAQ | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-ORRE | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-OROR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-ORGO | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-ORGR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-ORAQ | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GORE | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GOOR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GOGO | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GOGR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GOAQ | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GRRE | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GROR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GRGO | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GRGR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-GRAQ | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-AQRE | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-AQOR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-AQGO | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-AQGR | 20 (40 μL) | 200 μL |
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| APOA2-ITPR2-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes apolipoprotein (apo-) A-II, which is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. Defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia. [provided by RefSeq, Jul 2008]
Gene Symbol : APOA2
Gene Name : Apolipoprotein A2
Chromosome : CHR 1: 161,223,627-161,222,292
Locus : 1q23.3
The protein encoded by this gene belongs to the inositol 1,4,5-triphosphate receptor family, whose members are second messenger intracellular calcium release channels. These proteins mediate a rise in cytoplasmic calcium in response to receptor activated production of inositol triphosphate. Inositol triphosphate receptor-mediated signaling is involved in many processes including cell migration, cell division, smooth muscle contraction, and neuronal signaling. This protein is a type 2 receptor that consists of a cytoplasmic amino-terminus that binds inositol triphosphate, six membrane-spanning helices that contribute to the ion pore, and a short cytoplasmic carboxy-terminus. A mutation in this gene has been associated with anhidrosis, suggesting that intracellular calcium release mediated by this protein is required for eccrine sweat production. [provided by RefSeq, Apr 2015]
Gene Symbol : ITPR2
Gene Name : Inositol 1,4,5-trisphosphate receptor type 2
Chromosome : CHR 12: 268,331,97-263,353,36
Locus : 12p11.23
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