SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ZBTB20-PGD-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
ZBTB20-PGD-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015]
Gene Symbol : PGD
Gene Name : Phosphogluconate dehydrogenase
Chromosome : CHR 1: 103,989,91-104,205,10
Locus : 1p36.22
This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]
Gene Symbol : ZBTB20
Gene Name : Zinc finger and BTB domain containing 20
Chromosome : CHR 3: 115,147,279-114,314,499
Locus : 3q13.31
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