PEPCK-C rabbit pAb

PEPCK-C rabbit pAb

AO-06-ES3966-100

PEPCK-C rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES3966
Product namePEPCK-C rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other namePCK1; PEPCK1; Phosphoenolpyruvate carboxykinase, cytosolic [GTP]; PEPCK-C; Phosphoenolpyruvate carboxylase
Size100μL
Unit price ($)248
Human gene ID5105
Human Swiss-ProtP35558
SourceRabbit
IsotypeIgG
TargetPEPCK-C
Fields>>Glycolysis / Gluconeogenesis;>>Citrate cycle (TCA cycle);>>Pyruvate metabolism;>>Metabolic pathways;>>PPAR signaling pathway;>>FoxO signaling pathway;>>PI3K-Akt signaling pathway;>>AMPK signaling pathway;>>Insulin signaling pathway;>>Adipocytokine signaling pathway;>>Glucagon signaling pathway;>>Insulin resistance;>>Proximal tubule bicarbonate reclamation
Gene namePCK1
Protein namePhosphoenolpyruvate carboxykinase cytosolic [GTP]
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID18534
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9Z2V4
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID362282
Rat gene linkView Rat Gene
Rat Swiss-ProtP07379
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from the Internal region of human PCK1. AA range:491-540
SpecificityPEPCK-C Polyclonal Antibody detects endogenous levels of PEPCK-C protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)65kD
BackgroundThis gene is a main control point for the regulation of gluconeogenesis. The cytosolic enzyme encoded by this gene, along with GTP, catalyzes the formation of phosphoenolpyruvate from oxaloacetate, with the release of carbon dioxide and GDP. The expression of this gene can be regulated by insulin, glucocorticoids, glucagon, cAMP, and diet. Defects in this gene are a cause of cytosolic phosphoenolpyruvate carboxykinase deficiency. A mitochondrial isozyme of the encoded protein also has been characterized. [provided by RefSeq, Jul 2008],
Functioncatalytic activity:GTP + oxaloacetate = GDP + phosphoenolpyruvate + CO(2).,cofactor:Binds 1 manganese ion per subunit.,disease:Defects in PCK1 are the cause of cytosolic phosphoenolpyruvate carboxykinase deficiency (cytosolic PEPCK deficiency) [MIM:261680]. PEPCK deficiency is a metabolic disorder resulting from impaired gluconeogenesis. It is a rare disease with less than 10 cases reported in the literature. Clinical characteristics include hypotonia, hepatomegaly, failure to thrive, lactic acidosis and hypoglycaemia. Autoposy reveals fatty infiltration of both the liver and kidneys. The disorder is transmitted as an autosomal recessive trait.,enzyme regulation:Activity is affected by a number of hormones regulating this metabolic process (such as glucagon, insulin, or glucocorticoids).,function:Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP), the rate-limiti
Subcellular locationCytoplasm, cytosol . Endoplasmic reticulum . Phosphorylation at Ser-90 promotes translocation to the endoplasmic reticulum. .
ExpressionMajor sites of expression are liver, kidney and adipocytes.

Additional Images

Image 1
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Western Blot analysis of HeLa, MCF7 cells using PEPCK-C Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded rat-liver, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded rat-liver, antibody was diluted at 1:100
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Immunohistochemical analysis of paraffin-embedded mouse-liver, antibody was diluted at 1:100
: AO-06-ES3966-100
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Hurry! only 10 items left in stock.

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