product summary
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company name :
MyBioSource
product type :
ELISA/assay
product name :
Rat Glucose-6-Phosphatase, Catalytic ELISA Kit
catalog :
MBS097902
quantity :
48-Strip-Wells
price :
435 USD
more info or order :
product information
catalog number :
MBS097902
products type :
ELISA Kit
products full name :
Rat Glucose-6-Phosphatase, Catalytic ELISA Kit
products short name :
Glucose-6-Phosphatase, Catalytic
other names :
Glucose-6-phosphatase; Glucose-6-phosphatase; glucose-6-phosphatase; G6Pase; G-6-Pase; G6Pase-alpha; glucose-6-phosphatase alpha; glucose-6-phosphatase, catalytic subunit; Glucose-6-phosphatase alpha
products gene name :
G6PC
other gene names :
G6PC; G6PC; G6PT; GSD1; G6PC1; GSD1a; G6PT; G-6-Pase; G6Pase
uniprot entry name :
G6PC_HUMAN
reactivity :
Rat
sequence length :
357
specificity :
No significant cross-reactivity or interference between this analyte and analogues is observed.
storage stability :
Store all reagents at 2-8 degree C
other info1 :
Samples: Undiluted original Rat body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances. Assay Type: Sandwich. Detection Range: 3.12 U/L - 100 U/L. Sensitivity: 1.0U/L.
other info2 :
Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100].
products description :
Background/Introduction: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! This kit is intended to be used for determination the level of G6PC (hereafter termed "analyte") in undiluted original Rat body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances.
ncbi gi num :
206729864
ncbi acc num :
P35575.2
uniprot acc num :
P35575
ncbi mol weight :
40,484 Da
ncbi pathways :
AMPK Signaling Pathway (989139); AMPK Signaling Pathway (992181); Adipocytokine Signaling Pathway (83093); Adipocytokine Signaling Pathway (505); Carbohydrate Digestion And Absorption Pathway (170720); Carbohydrate Digestion And Absorption Pathway (170654); DNA Damage Response (only ATM Dependent) Pathway (198827); Disease Pathway (530764); FOXA2 And FOXA3 Transcription Factor Networks Pathway (137911); FoxO Family Signaling Pathway (138036)
ncbi summary :
Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.[provided by RefSeq, Feb 2011]
uniprot summary :
G6PC: Hydrolyzes glucose-6-phosphate to glucose in the endoplasmic reticulum. Forms with the glucose-6-phosphate transporter (SLC37A4/G6PT) the complex responsible for glucose production through glycogenolysis and gluconeogenesis. Hence, it is the key enzyme in homeostatic regulation of blood glucose levels. Defects in G6PC are the cause of glycogen storage disease type 1A (GSD1A). A metabolic disorder characterized by impairment of terminal steps of glycogenolysis and gluconeogenesis. Patients manifest a wide range of clinical symptoms and biochemical abnormalities, including hypoglycemia, severe hepatomegaly due to excessive accumulation of glycogen, kidney enlargement, growth retardation, lactic acidemia, hyperlipidemia, and hyperuricemia. Belongs to the glucose-6-phosphatase family. Protein type: Carbohydrate Metabolism - starch and sucrose; Phosphatase (non-protein); Membrane protein, integral; Carbohydrate Metabolism - glycolysis and gluconeogenesis; Transporter, SLC family; Endoplasmic reticulum; Membrane protein, multi-pass; Transporter; EC 3.1.3.9; Carbohydrate Metabolism - galactose. Chromosomal Location of Human Ortholog: 17q21. Cellular Component: endoplasmic reticulum membrane; integral to membrane; integral to endoplasmic reticulum membrane. Molecular Function: glucose-6-phosphatase activity; phosphate binding; phosphotransferase activity, alcohol group as acceptor. Biological Process: steroid metabolic process; glycogen metabolic process; response to food; phosphorylated carbohydrate dephosphorylation; glycogen catabolic process; multicellular organism growth; glucose 6-phosphate metabolic process; pathogenesis; glucose transport; glucose homeostasis; gluconeogenesis; cholesterol homeostasis; triacylglycerol metabolic process; urate metabolic process; glucose-6-phosphate transport; regulation of gene expression; hexose transport; carbohydrate metabolic process; transmembrane transport. Disease: Glycogen Storage Disease Ia
size1 :
48-Strip-Wells
price1 :
435 USD
size2 :
96-Strip-Wells
price2 :
600
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

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