CDH13 Antibody
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货号:CSB-PA005039GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P55290
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基因名:CDH13
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别名:CAD13_HUMAN antibody; Cadherin-13 antibody; CDH13 antibody; CDHH antibody; H-cadherin antibody; Heart cadherin antibody; P105 antibody; T cad antibody; T Cadherin antibody; T-cad antibody; T-cadherin antibody; Truncated cadherin antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Human CDH13
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免疫原种属:Homo sapiens (Human)
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抗体亚型:IgG
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纯化方式:Antigen Affinity Purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB,IHC
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Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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靶点详情
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功能:Cadherins are calcium-dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types. May act as a negative regulator of neural cell growth.
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基因功能参考文献:
- In this young Chinese population, CDH13 rs4783244 represents a key locus for cardiac structure, and confers stronger cardio-protection in longer sleep duration when contrasted with short sleep duration PMID: 29903569
- Polymorphism in CDH13 is associated with nephropathy in subjects with type 1 diabetes. PMID: 28499019
- The single nucleotide polymorphisms (SNPs) rs12596316AG genotype of the T-cadherin (CDH13) gene is associated with the susceptibility to metabolic syndrome (MS) among ethnic Han Chinese. PMID: 29419874
- the data suggests that the CDH13 T > A (rs11646213) polymorphism is associated with decreased risk of developing hypertension in the Mexican population PMID: 27682011
- nine ADHD candidate single nucleotide polymorphisms (SNPs) in seven genes were tested for association with PD in 5333 cases and 12,019 healthy controls. No significant association was observed. PMID: 28176268
- CDH13 genetic polymorphisms are associated with adiponectin levels and ischemic stroke. PMID: 28245897
- Study evaluated the associations between 6 SNPs in CDH13 and type 2 diabetes mellitus (T2DM) in a Han Chinese population. Results showed that the rs12596316 AG genotype was a risk genotype for the development of T2DM in the overdominant inheritance model; rs11646213, rs3865188, rs12444338, rs12051272, and rs7195409 had no observed associations with T2DM in terms of alleles, genotypes, and the various inheritance models. PMID: 28562572
- The methylation status of CDH13 promoter was strongly associated with breast cancer risk. However, CDH13 promoter methylation was not significantly related to the OS and DFS of breast cancer and may have limited prognostic value for breast cancer patients PMID: 27153114
- Studied the associations between genetic variants of CDH13 and type 2 diabetes (T2D), and its related parameters, in a Caucasian population. PMID: 27289142
- Compared with adjacent normal tissues, the methylation frequencies of WIF-1, RASSF1A, and CDH13 genes were significantly higher but the mRNA levels of these 3 genes were significantly lower in EC tissues. The survival rates of patients with WIF-1, RASSF1A, and CDH13 methylations were significantly lower than those of patients without methylation PMID: 27506957
- higher promoter methylation in colorectal cancer than in premalignant, normal, adjacent tissues; highest promoter methylation in poorly differentiated colorectal cancer PMID: 28121942
- CDH13 genetic variants determine Chinese individuals' susceptibility to chronic obstructive pulmonary disease (COPD) and thus are efficient genetic biomarkers for early detection of COPD. PMID: 26806298
- Strong Functional Association of adipor2 and cdh13 with adipoq PMID: 25388841
- CDH13 Polymorphisms are Associated with Adiponectin Levels and Metabolic Syndrome Traits Independently of Visceral Fat Mass. PMID: 26423718
- CDH13 locus variants and adiponectin levels are associated with circulating levels of cellular adhesion molecules and adiposity status in a differential manner that interacts with sex PMID: 26600672
- This study finding significant excess of rare nonsynonymous variants exclusive to European Americans smokers in CHD13. PMID: 25450229
- Data demonstrate for the first time that SHP1 methylation has high specificity for diagnosis of endometrial carcinoma, while CDH13 promoter methylation plays a role in the earlier stage. PMID: 26597461
- The present study identified a new genetic factor for CRC risk and an interaction between CDH13 and APN in CRC risk. These genetic factors may be useful for predicting CRC risk. PMID: 26362652
- The downregulation of T-cadherin may contribute to gastric cancer progression, representing a useful biomarker for predicting the biological behavior and prognosis of gastric cancer. PMID: 25847144
- Finnish prisoners, revealed that a monoamine oxidase A (MAOA) low-activity genotype (contributing to low dopamine turnover rate) as well as the CDH13 gene (coding for neuronal membrane adhesion protein) are associated with extremely violent behavior PMID: 25349169
- The genetic polymorphisms at the CDH13 locus independently affect the adiponectin levels, whereas the adiponectin levels exhibit a suppressive effect on the association between CDH13 locus variants and various metabolic phenotypes and metabolic syndrome PMID: 25875811
- The CDH13 rs11150556 CC genotype was associated with more hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder. PMID: 25739828
- CDH13 promoter methylation is associated with lung cancer. PMID: 25735345
- Aberrant promoter methylation of the cadherin 13 gene in serum is associated with prostate cancer. PMID: 25015764
- Our results suggested that negative T-cadherin expression has a worse prognosis in patients with axillary lymph node-positive breast cancer. PMID: 25677746
- down-regulation of adiponectin receptors (AdipoR1, R2, and T-cadherin) in osteoarthritic chondrocytes PMID: 24888493
- CDH13 DNA is methylated in only ten percent of cervical cancer patients. PMID: 22942707
- High frequency of CDH13 hypermethylation is associated with melanoma brain metastases. PMID: 24968695
- CDH13 methylation is a frequent event in non-muscle invasive bladder cancer. PMID: 25196672
- Several SNPs in the CDH13 promoter region are significantly associated with the level of DNA methylation at nearby CpG sites. PMID: 25543204
- T-cadherin regulates prostate cancer cell behavior by tuning the balance in EGFR/IGF-1R activity and enhancing the impact of IGF-1R PMID: 25381040
- High methylation level of CDH13 gene promoter region is associated with low drug sensitivity of non-small cell lung cancer. PMID: 24998565
- T-cadherin exhibited a state of insulin insensitivity as evidenced by attenuation of the ability of insulin to stimulate Akt/mTOR axis signaling, phosphorylation of MLC20 and MYPT1 PMID: 24815187
- Adiponectin/T-cadherin and apelin/APJ expression patterns were found to be inversely associated with human aortic and coronary atherosclerosis. PMID: 24675084
- CDH13 genotype may be a factor that affects not only the plasma level of HMWA but also the prognostic significance of HMWA. PMID: 24041676
- A non significant trend for higher levels of total adiponectin was observed in adult attention deficit hyperactivity disorder patients carrying CDH13 missense mutations compared to patients with wild type CDH13. PMID: 24559850
- The SNPs in ADP-ribosylation factor-like protein 15 (ARL15) and the T-cadherin (CDH13) genes did not exhibit significant association with individual metabolic traits in the T2DM and NDM groups. PMID: 24688318
- The SNPs most strongly associated in the single-marker analysis of the combined Danish samples were rs4757144 in ARNTL (P=3.78 x 10-6) and rs8057927 in CDH13. PMID: 23358160
- High CDH-13 expression is associated with melanoma. PMID: 23625515
- The results provide evidence that CDH13 variants are associated with metabolic traits and carotid atherosclerosis in Koreans. PMID: 24142632
- genome-wide association study in populations in Minnesota and Utah: Data suggest that SNPs on chromosome 12 and in CDH13 (H-cadherin) are associated with baseline circulating levels of adiponectin (and response of adiponectin levels to fenofibrate). PMID: 23149075
- high expressionsin uterine leiomyoma, associated with color Doppler flow imaging PMID: 23463326
- the frequency of coding CDH13 variants in adult attention deficit/hyperactivity disorder PMID: 23936508
- Cadherin 13 might play a role in the protoporphyrin (Pp)IX accumulation pathway and act as a negative regulator of 5-ALA-induced fluorescence in glioma cells. PMID: 24010971
- CDH13 variants strongly influence plasma total and high molecular weight adiponectin levels in East Asian populations but appear to alter adiponectin sensitivity, resulting in better metabolic health than expected based on circulating adiponectin levels. PMID: 24009259
- T-cadherin translocation to cell-cell contacts is sensitive to the activity status of EGFR, requires lipid raft domain integrity and actin filament polymerization, and crucial intracellular signalling mediators include Rac1 and p38MAPK. PMID: 23411345
- Downregulated expression of CDH13 is associated with increased invasion of bladder transitional cell carcinoma PMID: 23235385
- Data indicate that T-cadherin-silencing promotes experimental metastasis of squamous cell carcinoma (SCC). PMID: 23369463
- The present study investigated transcriptional regulation of CDH13 in melanoma. Found an inverse correlation between BRN2 and T-cadherin protein and transcript expression in melanoma. PMID: 23069940
- This study identifying loci for aADHD and led to the identification of CHD13 as novel genes associated with ADHD across the lifespan. PMID: 22105624
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亚细胞定位:Cell membrane; Lipid-anchor, GPI-anchor.
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组织特异性:Highly expressed in heart. In the CNS, expressed in cerebral cortex, medulla, hippocampus, amygdala, thalamus and substantia nigra. No expression detected in cerebellum or spinal cord.
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数据库链接:
HGNC: 1753
OMIM: 601364
KEGG: hsa:1012
STRING: 9606.ENSP00000408632
UniGene: Hs.654386
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