Product: DBH Recombinant Rabbit mAb
Catalog: BF4401
Description: Rabbit monoclonal antibody to DBH
Application: WB IHC
Reactivity: Human, Mouse, Rat
Mol.Wt.: 75-80 kDa(Observed); 69kD(Calculated).
Uniprot: P09172

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Product Info

Source:
Rabbit IgG
Application:
WB 1:1000, IHC 1:200-1:2000
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*Tips:

WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.

Reactivity:
Human, Mouse, Rat
Clonality:
Monoclonal [ReFirm23851]
Specificity:
DBH Recombinant Rabbit mAb detects endogenous levels of DBH.
Conjugate:
Unconjugated.
Purification:
Affinity-chromatography.
Storage:
Rabbit IgG in Tris-Glycine (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
Alias:

Fold/Unfold

dbh; DBM; Dopamine beta hydroxylase; Dopamine beta monooxygenase; Dopamine beta-hydroxylase (dopamine beta-monooxygenase); Dopamine beta-monooxygenase; DOPO_HUMAN; OTTHUMP00000022501; Soluble dopamine beta-hydroxylase;

Immunogens

Immunogen:

A synthetic peptide from human DBH

Uniprot:
Gene(ID):
Description:
The protein encoded by this gene is an oxidoreductase belonging to the copper type II,ascorbate-dependent monooxygenase family. The encoded protein,expressed in neuroscretory vesicles and chromaffin granules of the adrenal medulla,catalyzes the conversion of dopamine to norepinephrine,which functions as both a hormone and as the main neurotransmitter of the sympathetic nervous system. The enzyme encoded by this gene exists exists in both soluble and membrane-bound forms,depending on the absence or presence,respectively,of a signal peptide. Mutations in this gene cause dopamine beta-hydroxylate deficiency in human patients,characterized by deficits in autonomic and cardiovascular function,including hypotension and ptosis. Polymorphisms in this gene may play a role in a variety of psychiatric disorders.
Sequence:
MPALSRWASLPGPSMREAAFMYSTAVAIFLVILVAALQGSAPRESPLPYHIPLDPEGSLELSWNVSYTQEAIHFQLLVRRLKAGVLFGMSDRGELENADLVVLWTDGDTAYFADAWSDQKGQIHLDPQQDYQLLQVQRTPEGLTLLFKRPFGTCDPKDYLIEDGTVHLVYGILEEPFRSLEAINGSGLQMGLQRVQLLKPNIPEPELPSDACTMEVQAPNIQIPSQETTYWCYIKELPKGFSRHHIIKYEPIVTKGNEALVHHMEVFQCAPEMDSVPHFSGPCDSKMKPDRLNYCRHVLAAWALGAKAFYYPEEAGLAFGGPGSSRYLRLEVHYHNPLVIEGRNDSSGIRLYYTAKLRRFNAGIMELGLVYTPVMAIPPRETAFILTGYCTDKCTQLALPPSGIHIFASQLHTHLTGRKVVTVLVRDGREWEIVNQDNHYSPHFQEIRMLKKVVSVHPGDVLITSCTYNTEDRELATVGGFGILEEMCVNYVHYYPQTQLELCKSAVDAGFLQKYFHLINRFNNEDVCTCPQASVSQQFTSVPWNSFNRDVLKALYSFAPISMHCNKSSAVRFQGEWNLQPLPKVISTLEEPTPQCPTSQGRSPAGPTVVSIGGGKG

Research Backgrounds

Function:

Conversion of dopamine to noradrenaline.

PTMs:

N-glycosylated.

Proteolytic cleavage after the membrane-anchor leads to the release of the soluble form.

Subcellular Location:

Cytoplasmic vesicle>Secretory vesicle lumen. Cytoplasmic vesicle>Secretory vesicle>Chromaffin granule lumen. Secreted.

Cytoplasmic vesicle>Secretory vesicle membrane>Single-pass type II membrane protein. Cytoplasmic vesicle>Secretory vesicle>Chromaffin granule membrane>Single-pass type II membrane protein.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
Family&Domains:

Belongs to the copper type II ascorbate-dependent monooxygenase family.

Research Fields

· Metabolism > Amino acid metabolism > Tyrosine metabolism.

· Metabolism > Global and overview maps > Metabolic pathways.

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