Recombinant Human Aromatic-L-amino-acid decarboxylase (DDC)
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中文名称:Recombinant Human Aromatic-L-amino-acid decarboxylase(DDC),Yeast
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货号:CSB-YP006583HU
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规格:
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来源:Yeast
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其他:
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中文名称:Recombinant Human Aromatic-L-amino-acid decarboxylase(DDC),Yeast
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货号:CSB-EP006583HU
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规格:
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来源:E.coli
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其他:
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中文名称:Recombinant Human Aromatic-L-amino-acid decarboxylase(DDC),Yeast
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货号:CSB-EP006583HU-B
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规格:
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来源:E.coli
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共轭:Avi-tag Biotinylated
E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.
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其他:
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中文名称:Recombinant Human Aromatic-L-amino-acid decarboxylase(DDC),Yeast
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货号:CSB-BP006583HU
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规格:
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来源:Baculovirus
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其他:
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中文名称:Recombinant Human Aromatic-L-amino-acid decarboxylase(DDC),Yeast
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货号:CSB-MP006583HU
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规格:
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来源:Mammalian cell
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其他:
产品详情
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纯度:>85% (SDS-PAGE)
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基因名:DDC
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Uniprot No.:
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别名:AADC; Aromatic L Amino Acid Decarboxylase; Aromatic-L-amino-acid decarboxylase; DDC; DDC_HUMAN; DOPA decarboxylase (aromatic L-amino acid decarboxylase); DOPA decarboxylase
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种属:Homo sapiens (Human)
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蛋白长度:Full length protein
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表达区域:1-480
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氨基酸序列MNASEFRRRG KEMVDYMANY MEGIEGRQVY PDVEPGYLRP LIPAAAPQEP DTFEDIINDV EKIIMPGVTH WHSPYFFAYF PTASSYPAML ADMLCGAIGC IGFSWAASPA CTELETVMMD WLGKMLELPK AFLNEKAGEG GGVIQGSASE ATLVALLAAR TKVIHRLQAA SPELTQAAIM EKLVAYSSDQ AHSSVERAGL IGGVKLKAIP SDGNFAMRAS ALQEALERDK AAGLIPFFMV ATLGTTTCCS FDNLLEVGPI CNKEDIWLHV DAAYAGSAFI CPEFRHLLNG VEFADSFNFN PHKWLLVNFD CSAMWVKKRT DLTGAFRLDP TYLKHSHQDS GLITDYRHWQ IPLGRRFRSL KMWFVFRMYG VKGLQAYIRK HVQLSHEFES LVRQDPRFEI CVEVILGLVC FRLKGSNKVN EALLQRINSA KKIHLVPCHL RDKFVLRFAI CSRTVESAHV QRAWEHIKEL AADVLRAERE
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蛋白标签:Tag type will be determined during the manufacturing process.
The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially. -
产品提供形式:Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand. -
复溶:We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
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储存条件:Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
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保质期:The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C. -
货期:Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
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注意事项:Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
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Datasheet :Please contact us to get it.
相关产品
靶点详情
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功能:Catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine, L-5-hydroxytryptophan to serotonin and L-tryptophan to tryptamine.
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基因功能参考文献:
- We found the suicide-associated gene coexpression network. The reconstructed network consisted of 104 genes. Topological analysis showed that in total, CCK, INPP1, DDC, and NPY genes are the most fundamental hubs in the network PMID: 29381655
- IKZF1 rs10235796 C allele, IKZF1 rs6964969A>G, CDKN2A rs3731246 G>C, and CDKN2A rs3731246 C allele were signi fi cantly associated with Acute Lymphoblastic Leukemia in Yemenis of Arab-Asian descent. Borderline association found in IKZF1 rs4132601 T>G variant. No associations found with IKZF1 rs11978267 or rs7789635, DDC rs3779084; rs880028; rs7809758, CDKN2A rs3731217, CEBPE rs2239633; rs12434881 PMID: 28768142
- The data provide evidence for cis-acting, functional common polymorphisms in the DOPA decarboxylase gene in the human ventral striatum. PMID: 26924680
- Human histidine decarboxylase (HDC) and dopa decarboxilase (DDC) are highly homologous enzymes responsible for the synthesis of biogenic amines (BA) like histamine, and serotonin and dopamine, respectively. This review summarizes the analogies and differences in their origin as well as their common pathophysiological scenarios. [review] PMID: 27769832
- Newborn screening of AADC deficiency was achieved with a 100% positive-predictive rate. An association for gestational age could be further elucidated. PMID: 27216367
- SNP rs10499695 located intronically in the gene DDC, (DOPA decarboxylase) is significantly associated with cognitive performance in diabetes 2. PMID: 27066308
- Molecular characteristic and physiological role of DOPA-decarboxylase is reviewed. PMID: 28100850
- We found that only the modified U1 snRNA (IVS-AAA) that completely matched both the intronic and exonic U1 binding sequences of the mutated DDC gene could correct splicing errors of either the mutated human DDC minigene or the mouse artificial splicing construct in vitro PMID: 27658936
- The results of this study showed that Lack of Association Between Polymorphisms in Dopa decarboxylase Genes With Childhood PMID: 26337060
- The data showed that L-DOPA decarboxylase constitutes a highly promising molecular marker for renal cell carcinoma. PMID: 25721989
- gene study of 987 BPD cases and 1110 healthy controls found an association between BPD [ borderline personality disorder ]and single nucleotide polymorphism rs12718541 in the dopa decarboxylase gene PMID: 25017620
- Results revealed the general picture of structural and/or functional effects of each DDC mutation linked to AADC deficiency mutations and help to guide therapeutic decision and prevent inappropriate use of treatment regiments. PMID: 24865461
- A novel homozygous DDC variant in syndromic intellectual disability patients, c.1123C>T, resulting in p.Arg375Cys missense substitution. PMID: 25597765
- Results indicate that miR-145 has the ability to regulate DDC mRNA expression and potentially this occurs by recognizing its mRNA as a target. PMID: 25445287
- Our results suggest that DDC may be a genetic modifier of the l-dopa response in Parkinson's disease PMID: 24216088
- 8 SNPs in DDC gene showed significant associations with MaxDrinks. PMID: 23953852
- Common allelic variants in the DDC gene may be involved in autism susceptibility. PMID: 22397633
- The data of this study confirm histidine decarboxylase deficiency as a rare cause of TS and identify HA-DA interactions in the basal ganglia as an important locus of pathology. PMID: 24411733
- Absorbance and fluorescence titrations of hDDC-bound coenzyme identify a single pK(spec) of ~7.2. PMID: 23781496
- This study provides the first evidence for the involvement of the DDC gene in alerting attention PMID: 23276884
- The aim of the current study was to analyze the DDC mRNA expression in head and neck squamous cell carcinoma (HNSCC) patients. DDC mRNA levels were lower in squamous cell carcinomas of the larynx and tongue than in adjacent non-cancerous tissue specimens. PMID: 23083099
- This work is the first to shed light on the potential clinical usefulness of DDC, as an efficient tumor biomarker in gastric cancer. PMID: 23064786
- This is the first study indicating the potential of DDC expression as a novel prognostic biomarker in patients with PCa who have undergone radical prostatectomy PMID: 22571720
- In regular smokers, variability at the locus marked by rs3779084 in the dopa decarboxylase gene appears to index biologically based individual differences in the motivation to consume alcohol. PMID: 21797889
- we report biochemical and bioinformatic analyses of the human wild-type dopa decarboxylase and the pathogenic variants G102S, F309L, S147R and A275T whose mutations concern amino acid residues at or near the active site. PMID: 21541720
- analysis of how the open conformation of human DOPA decarboxylase reveals the mechanism of PLP addition to Group II decarboxylases PMID: 22143761
- Results describe the cellular topology of active human L-dopa decarboxylase. PMID: 21479916
- These results suggested that TonEBP played an important role in the epithelial cells of renal proximal tubule upon hypertonic stress by enhancing AAD expression, which could promote dopamine secretion to negative regulate Na+/K+-ATPase activity. PMID: 21982764
- the human DDC gene undergoes complex processing, leading to the formation of multiple mRNA isoforms in tumor cells PMID: 20535562
- Normal or increased levels of urinary dopamine are found in the majority of AADC-deficient patientsNormal or increased levels of urinary dopamine are found in the majority of AADC-deficient patients PMID: 20832343
- The intronic Single Nucleotide Polymorphism at the is significantly associated to the Spielberger State-Trait Anxiety Inventory anxiety scores after multiple testing correction. PMID: 20092830
- Dopa decarboxylase mRNA expression may be a novel potential tissue biomarker in prognosis of colorectal adenocarcinoma patient survival. PMID: 20424616
- The expression of enzymatically active DDC shows the endogenous production of dopamine in U937 cells and raises new questions about the enzyme's involvement in immune responses. PMID: 19800137
- gene promoter directs transgene expression to the adult floor plate and aminergic nuclei induced by the isthmus. PMID: 11750071
- findings suggest that the DDC gene is unlikely to play a major role in the development of autism in our data set PMID: 11992572
- Results do not support an involvement of the 1-bp or 4-bp deletion within the DDC gene in the etiology of affective disorders. PMID: 12116187
- DDC might confer susceptibility to bipolar affective disorder predominantly when paternally transmitted PMID: 12555230
- This enzyme is cloned from and expressed in placenta. PMID: 12718431
- We report three siblings who showed the clinical phenotype to be caused by aromatic L-amino acid decarboxylase deficiency. Molecular characterization showed a homozygous point mutation (c.387 G-->A) in exon 3. PMID: 14991824
- Polymorphisms studied do not play a major role in paranoid schizophrenia pathogenesis in the population investigated. PMID: 15318031
- dopamine decarboxylase mRNA in neuroblastoma patients could be a potential marker for minimal residual disease PMID: 15322424
- Detection of a new alternative splicing event within the coding region of the human dopa decarboxylase (DDC) mRNA, suggests that the single copy human DDC gene undergoes complex processing leading to the formation of multiple mRNA isoforms. PMID: 15532536
- Single nucleotide polymorphisms in the dopa decarboxylase gene is associated with nicotine dependence PMID: 15879433
- Immunohistochemical detection of DOPA decarboxylase shows diffuse staining of Langerhans islets in congenital hyperinsulinism. PMID: 16403819
- association of alleles and haplotypes at the DOPA decarboxylase (DDC) locus with the DSM-IV diagnosis of nicotine dependence PMID: 16740595
- Association of the DOPA decarboxylase (DDC) gene on chromosome 7p11 with measures of nicotine dependence. PMID: 17184203
- Autoantibodies to the COOH-terminal region induce a significant inhibition of enzymatic activity. PMID: 17200166
- Expands clinical spectrum of AADC deficiency and contributes to the knowledge of the genotype and phenotype correlation for the DDC gene. PMID: 17533144
- The DDC gene was strongly associated with both adulthood (P=0.00053; odds ratio (OR)=2.17) and childhood ADHD (P=0.0017; OR=1.90) PMID: 17938636
- study does not support the involvement of tyrosine hydroxylase gene variants as major contributors to suicide, whereas dopa decarboxylase variants could mediate some features related to suicide and be involved in violent suicidal behavior PMID: 17948905
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相关疾病:Aromatic L-amino-acid decarboxylase deficiency (AADCD)
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蛋白家族:Group II decarboxylase family
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数据库链接:
HGNC: 2719
OMIM: 107930
KEGG: hsa:1644
STRING: 9606.ENSP00000350616
UniGene: Hs.359698
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