PD-ECGF rabbit pAb

PD-ECGF rabbit pAb

AO-06-ES4144-50

PD-ECGF rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES4144
Product namePD-ECGF rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;IHC;IF;ELISA
Other nameTYMP; ECGF1; Thymidine phosphorylase; TP; Gliostatin; Platelet-derived endothelial cell growth factor; PD-ECGF; TdRPase
Size50μL
Unit price ($)148
Human gene ID1890
Human Swiss-ProtP19971
SourceRabbit
IsotypeIgG
TargetPD-ECGF
Fields>>Pyrimidine metabolism;>>Drug metabolism - other enzymes;>>Metabolic pathways;>>Nucleotide metabolism;>>Bladder cancer
Gene nameTYMP
Protein nameThymidine phosphorylase
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID72962
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ99N42
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID315219
Rat gene linkView Rat Gene
Rat Swiss-ProtQ5FVR2
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from the N-terminal region of human TYMP. AA range:11-60
SpecificityPD-ECGF Polyclonal Antibody detects endogenous levels of PD-ECGF protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1/100-1/300. 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)50kD
BackgroundThis gene encodes an angiogenic factor which promotes angiogenesis in vivo and stimulates the in vitro growth of a variety of endothelial cells. It has a highly restricted target cell specificity acting only on endothelial cells. Mutations in this gene have been associated with mitochondrial neurogastrointestinal encephalomyopathy. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Apr 2012],
Functioncatalytic activity:Thymidine + phosphate = thymine + 2-deoxy-alpha-D-ribose 1-phosphate.,disease:Defects in TYMP are the cause of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) [MIM:603041]; also known as myoneurogastrointestinal encephalomyopathy. MNGIE is an autosomal recessive disease associated with multiple deletions of skeletal muscle mitochondrial DNA (MtDNA). It is clinically characterized by onset between the second and fifth decades of life, ptosis, progressive external ophthalmoplegia, gastrointestinal dysmotility (often pseudoobstruction), diffuse leukoencephalopathy, thin body habitus, peripheral neuropathy, and myopathy.,function:Catalyzes the reversible phosphorolysis of thymidine. The produced molecules are then utilized as carbon and energy sources or in the rescue of pyrimidine bases for nucleotide synthesis.,function:May have a role in maintaining the in
Subcellular locationcytosol,
ExpressionBrain,Lung,Placenta,Synovial membrane tissue,

Additional Images

Image 1
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Western Blot analysis of MCF-7, 293 cells using PD-ECGF Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
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Immunohistochemical analysis of paraffin-embedded Human kidney. 1, Antibody was diluted at 1:200(4° overnight). 2, High-pressure and temperature EDTA, pH8.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 30min).
: AO-06-ES4144-50
: 10 Items
Hurry! only 10 items left in stock.

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