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Catalog: YT1911
Size
Price
Status
Qty.
200μL
$450.00
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100μL
$280.00
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40μL
$150.00
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Main Information
Target

GK1/3

Host Species

Rabbit

Reactivity

Human, Rat, Mouse,

Applications

WB, IHC, IF, ELISA

MW

61kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:40000; IF 1:50-200
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
GK1/3 Polyclonal Antibody detects endogenous levels of GK1/3 protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
61kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human GK3. AA range:21-70
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Specificity:
GK1/3 Polyclonal Antibody detects endogenous levels of GK1/3 protein.
show all
Gene Name:
GK/GK3P
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Protein Name:
Putative glycerol kinase 3
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Other Name:
GK ;
Glycerol kinase ;
GK ;
Glycerokinase ;
ATP:glycerol 3-phosphotransferase ;
GK3P ;
GKP3 ;
GKTB ;
Putative glycerol kinase 3 ;
GK 3 ;
Glycerokinase 3 ;
ATP:glycerol 3-phosphotransferase 3 ;
Glycerol kinase ;
testis specific 1
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Database Link:
Organism Gene ID SwissProt
Human 2713; P32189;Q14409;
Background:
The 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],
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Function:
Catalytic 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. Isoforms 2 and 3 are expressed specifically in testis and fetal liver, but not in the adult liver.,
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Cellular Localization:
Mitochondrion 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.
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Tissue Expression:
Highly 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.
show all
Research Areas:
>>Glycerolipid metabolism ;
>>Metabolic pathways ;
>>PPAR signaling pathway
show all
Catalog: YT1911
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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