GK1 rabbit pAb

GK1 rabbit pAb

AO-06-ES2428-50

GK1 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES2428
Product nameGK1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IF;ELISA
Other nameGK; Glycerol kinase; GK; Glycerokinase; ATP:glycerol 3-phosphotransferase
Size50μL
Unit price ($)148
Human gene ID2710
Human Swiss-ProtP32189
SourceRabbit
IsotypeIgG
TargetGK1
Fields>>Glycerolipid metabolism;>>Metabolic pathways;>>PPAR signaling pathway
Gene nameGK
Protein nameGlycerol kinase
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID14933
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ64516
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID79223
Rat gene linkView Rat Gene
Rat Swiss-ProtQ63060
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human GK. AA range:461-510
SpecificityGK1 Polyclonal Antibody detects endogenous levels of GK1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunofluorescence: 1/200 - 1/1000. 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)57kD
BackgroundThe protein encoded by this gene belongs to the FGGY kinase family. This protein is a key enzyme in the regulation of glycerol uptake and metabolism. It catalyzes the phosphorylation of glycerol by ATP, yielding ADP and glycerol-3-phosphate. Mutations in this gene are associated with glycerol kinase deficiency (GKD). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011],
Functioncatalytic activity:ATP + glycerol = ADP + sn-glycerol 3-phosphate.,caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease:Defects in GK are the cause of GK deficiency (GKD) [MIM:307030]. This disease can be either symptomatic with episodic metabolic and CNS decompensation or asymptomatic with hyperglycerolemia and hyperglyceroluria only.,function:Key enzyme in the regulation of glycerol uptake and metabolism.,pathway:Polyol metabolism; glycerol degradation via glycerol kinase pathway; sn-glycerol 3-phosphate from glycerol: step 1/1.,similarity:Belongs to the FGGY kinase family.,subcellular location:In sperm and fetal tissues, the majority of the enzyme is bound to mitochondria, but in adult tissues, such as liver found in the cytoplasm.,tissue specificity:Highly expressed in the liver, kidney and testis
Subcellular locationMitochondrion outer membrane; Peripheral membrane protein; Cytoplasmic side. Cytoplasm. In sperm and fetal tissues, the majority of the enzyme is bound to mitochondria, but in adult tissues, such as liver found in the cytoplasm.
ExpressionHighly expressed in the liver, kidney and testis. Isoform 2 and isoform 3 are expressed specifically in testis and fetal liver, but not in the adult liver.

Additional Images

Image 1
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Western Blot analysis of various cells using GK1 Polyclonal Antibody diluted at 1:2000
Image 2
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Immunofluorescence analysis of HeLa cells, using GK Antibody. The picture on the right is blocked with the synthesized peptide.
Image 3
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Western blot analysis of lysates from 293 and Jurkat cells, using GK Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES2428-50
: 10 Items
Hurry! only 10 items left in stock.

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