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DOPA Decarboxylase Rabbit pAb

DOPA Decarboxylase Rabbit pAb

     
  • 1 - DOPA Decarboxylase Rabbit pAb AP52155
    Sample:
    Lane 1: Cerebrum (Mouse) Tissue Lysate at 40 ug
    Lane 2: adrenal gland (Mouse) TissueLysate at 40 ug
    Lane 3: Cerebrum (Rat) Tissue Lysate at 40 ug
    Lane 4: adrenal gland (Rat) Tissue Lysate at 40 ug
    Lane 5: SH-SY5Y (Human) Cell Lysate at 30 ug
    Lane 6: HepG2 (Human) Cell Lysate at 30 ug
    Lane 7: Jurkat (Human) Cell Lysate at 30 ug
    Lane 8: A549 (Human) Cell Lysate at 30 ug
    Primary: Anti-DOPA Decarboxylase (AP52155) at 1/1000 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 53 kD
    Observed band size: 50 kD
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB
Primary Accession P20711
Reactivity Rat, Human, Mouse
Host Rabbit
Clonality Polyclonal
Calculated MW 53926 Da
Physical State Liquid
Immunogen KLH conjugated synthetic peptide derived from human DDC
Epitope Specificity 201-300/480
Isotype IgG
Purity affinity purified by Protein A
Buffer 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
DISEASE Defects in DDC are the cause of aromatic L-amino-acid decarboxylase deficiency (AADCD) [MIM:608643]. AADCD deficiency is an inborn error in neurotransmitter metabolism that leads to combined serotonin and catecholamine deficiency. It causes developmental and psychomotor delay, poor feeding, lethargy, ptosis, intermittent hypothermia, gastrointestinal disturbances. The onset is early in infancy and inheritance is autosomal recessive.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Background Descriptions bs-0180P is one synthetic peptide derived from human DDC. DOPA decarboxylase is an enzyme implicated in 2 metabolic pathways, synthesizing 2 important neurotransmitters: dopamine and serotonin which both play key roles in many clinical disorders, including Parkinson's disease. Following the hydroxylation of tyrosine to form L dihydroxyphenylalanine (LDOPA), catalyzed by tyrosine hydroxylase, DDC decarboxylates LDOPA to form dopamine. This neurotransmitter is found in different areas of the brain and is particularly abundant in basal ganglia. Dopamine is also produced by DDC in the sympathetic nervous system and is the precursor of the catecholaminergic hormones, noradrenaline and adrenaline in the adrenal medulla. In the nervous system, tryptophan hydroxylase produces 5 OH tryptophan, which is decarboxylated by DDC, giving rise to serotonin. DDC is a homodimeric, pyridoxal phosphate dependent enzyme.
Additional Information
Gene ID 1644
Other Names Aromatic-L-amino-acid decarboxylase, AADC, 4.1.1.28, DOPA decarboxylase, DDC, DDC {ECO:0000303|PubMed:15532536, ECO:0000312|HGNC:HGNC:2719}
Dilution WB=1:500-2000
StorageStore at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name DDC {ECO:0000303|PubMed:15532536, ECO:0000312|HGNC:HGNC:2719}
Function Catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine and L-5-hydroxytryptophan to serotonin.
Tissue Location [Isoform 2]: High expression in kidney.
Research Areas

BACKGROUND

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

REFERENCES

Ichinose H.,et al.Biochem. Biophys. Res. Commun. 164:1024-1030(1989).
Scherer L.J.,et al.Genomics 13:469-471(1992).
Sumi-Ichinose C.,et al.Biochemistry 31:2229-2238(1992).
Vassilacopoulou D.S.,et al.Neurochem. Res. 29:1817-1823(2004).
Hillier L.W.,et al.Nature 424:157-164(2003).

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