CAPN10 Antibody, FITC conjugated

說明書

中文名稱：

CAPN10兔多克隆抗體, FITC偶聯
貨號：

CSB-PA864027LC01HU
規格：

￥880
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) CAPN10 Polyclonal antibody
Uniprot No.：

Q9HC96
基因名：

CAPN10
別名：

Calcium activated neutral protease antibody; Calcium activated neutral proteinase 10 antibody; Calcium-activated neutral proteinase 10 antibody; calpain like protease CAPN10 antibody; Calpain-10 antibody; Calpain10 antibody; CAN10_HUMAN antibody; CANP 10 antibody; CANP10 antibody; CAPN 10 antibody; CAPN10 antibody; EC 3.4.22. antibody; KIAA1845 antibody; NIDDM1 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Calpain-10 protein (1-287AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

FITC
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

Antigen Affinity Purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
產品提供形式：

Liquid
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

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.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

功能：

Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. May play a role in insulin-stimulated glucose uptake.
基因功能參考文獻：
1. This study provides evidence that SNP43 (G/A) in the CAPN10 gene increases the risk of cognitive impairment in cerebral small vessel disease patients. PMID: 30014550
2. The 3R/3R genotype of the indel-19 variant of the CAPN-10 gene influenced increased glucose levels in these Mexican women with gestational diabetes mellitus. PMID: 29506634
3. TCF7L2 rs7903146 and 112/112 haplotype of CAPN10 might be associated with gestational diabetes risks. [meta-analysis] PMID: 28277135
4. association between SNP 63 of CAPN10 and gestational diabetes mellitus is only significant in the heterozygous model PMID: 27324783
5. There were significant differences between the type 2 diabetes mellitus patients and controls in the risk allele distributions of rs3792267 (CAPN10) (P = 0.002), rs1501299 (APM1) (P = 0.017), and rs3760776 (FUT6) (P = 0.031). PMID: 27374856
6. The study results were suggestive of a positive association between Gly972Arg of IRS1 and PCOS in the south Indian population, while INS, IRS2, PPAR-G and CAPN10 failed to show any association with PCOS in our studied population. PMID: 28360393
7. These findings indicate that the Calpain-10 SNP 43 may be related to obstructive sleep apnea/hypopnea syndrome with ischemic stroke, with SNP 43 GG genotype as a risk factor for obstructive sleep apnea/hypopnea with ischemic stroke PMID: 28422847
8. Subjects with the GG genotype of the rs2975762 variant of the CAPN10 gene were better responders to dietary intervention, showing increased HDL-C concentrations from the first month of treatment PMID: 25238846
9. due to its association with androgen excess in phenotype A, CAPN 10 gene polymorphism UCSNP-43 could be used as a genetic marker for CVD in young PCOS women. PMID: 26376770
10. genetic association studies in Asian populations: Data suggest that an SNP in CAPN10 (SNP43 G>A, rs3792267) is associated with type 2 diabetes in Asian populations, especially in Chinese populations. [META-ANALYSIS] PMID: 25382134
11. SNP-63 and indel-19 variant of the CAPN10 gene do not represent a risk factor for polycystic ovary syndrome in Mexican women of reproductive age. PMID: 25982606
12. Data indicate no association between calpain 10 (CAPN10) polymorphisms and type 2 diabetes mellitus. PMID: 25867367
13. 121 haplotype and 122/121 haplotype combination of SNP-19, -44 and -63 in the Calpain-10 gene are associated with the development of type 2 diabetes in Turkish patients. PMID: 24802731
14. Different mutations in CAPN10 have already been found in three independent Iranian families PMID: 25773692
15. This work confirms the association of CAPN10 gene with metabolic components in PCOS and highlights the role of haplotypes as strong and efficient genetic markers. PMID: 24993116
16. The present study provides the first observation of an association between a variant in CAPN10 gene and the response to metformin therapy in patients with type 2 diabetes PMID: 25327507
17. Genotype I/I of SNP19 in CAPN10 was significantly associated with excess weight in Colombian patients 10-18 years of age even those with physically active lifestyles. PMID: 25504243
18. SNP-19 in CAPN10 may participate in the development of diabetes mellitus type 2 PMID: 25617558
19. We replicated the significant association of rs1801278 and rs3792267 SNPs of the IRS1 and CAPN10 genes with T2DM in the population of Hyderabad. PMID: 24612564
20. results of present meta-analysis indicate an association of T2D with carriers of DD genotype of CAPN10 I/D polymorphism PMID: 24429295
21. Calpain-10 SNP43 and SNP19 polymorphisms are associated with colorectal cancer. PMID: 24377587
22. Variations of SNP-43, -63 and Indel-19 of CAPN10 were not associated with an increased risk of developing gestational diabetes mellitus. PMID: 24266779
23. Calpain 10 shows association between the single nucleotide polymorphism (SNP)-43, but not SNP-19 nor -63, and type 2 diabetes mellitus in the Kurdish ethnic group of West Iran PMID: 24779302
24. Used homology modelling technique to study the 3D structure of calpain-10 from Homo sapiens and its interaction with the protease inhibitor SNJ-1715. PMID: 24034724
25. Polymorphisms in the Calpain-10 gene may be risk factors for PCOS, especially among Asian populations.[meta-analysis] PMID: 23994294
26. Significant association of SNP -43 in CAPN10 with the risk of cardiovascular disease coexisting with T2 Diabetes mellitus. PMID: 23021796
27. GAEC1 regulates the expression of CAPN10 in esophageal squamous cell carcinoma. Calpain 10 expression is a potential prognostic marker. PMID: 23687414
28. We identified reduced Calpain-10 expression in a pediatric population with overweight and obese phenotypes. PMID: 23262350
29. analysis of copy number variation of CAPN10 in Thais with type 2 diabetes by multiplex PCR and denaturing high performance liquid chromatography PMID: 22796443
30. CAPN10 SNPs and haplotypes are associated with polycystic ovary syndrome among South Indian Women PMID: 22384174
31. Studies indicate UCSNP-63 of CAPN 10 gene was significantly associated with polycystic ovary syndrome (PCOS). PMID: 21906115
32. CAPN-10 gene SNP-56 plays a role in glucose and lipid metabolism in Chinese PCOS patients but does not contribute to the genetic susceptibility of PCOS. PMID: 18683748
33. CAPN10 SNP-19 is associated with glucose metabolism disorders in pregnant women. PMID: 19570442
34. This study raises the possibility that the 2111 haplotype of SNPs -44, -43, -19, and -63 may be associated with type 2 diabetes mellitus, although none of these SNPs may be individually associated with diabetes. PMID: 20667559
35. genetic association studies in a European cohort: CAPN10 SNP (rs2953171) may influence insulin sensitivity by interacting with plasma fatty acid composition in subjects with metabolic syndrome PMID: 21389182
36. Calpain 10 gene polymorphism is modifying laryngeal cancer risk and mortality in Spanish population. PMID: 20848425
37. calpain 10 UCSNP-19 polymorphism and haplotype 111 contribute to the risk of type 2 diabetes (T2DM) in Tunisian subjects but no significant association between calpain 10 diplotypes and T2DM was demonstrated PMID: 20570542
38. variation in CAPN10 may be associated with increased risk of pancreatic cancer among smokers PMID: 20178008
39. SNP-44 polymorphism of the calpain-10 gene has a significant association with T2DM patients in the Gaza strip PMID: 20881413
40. Meta-analysis and uncategorized study of gene-disease association. (HuGE Navigator) PMID: 20923526
41. Certain three window haplotypes may confer increased risk for T2DM and others may be protective suggesting that genetic variation in CAPN10 gene may be one factor involved in the aetiology of T2DM in Irish adults. PMID: 20119856
42. CAPN10 gene may play an important role in the pathogenesis of impaired fasting glucose or impaired glucose tolerance in patients with esential hypertension. PMID: 20406624
43. the most common haplotype 121 (OR = 0.70 95% CI: 0.50-0.99) was associated with a reduced risk for type 2 diabetes in East Indian population PMID: 20368234
44. Patients' higher body mass index and SNP-63 minor T allele carrier status were identified as independent posttransplant diabetes mellitus risk factors. PMID: 19752882
45. CAPN10 UCSNP-19 variant, and the 111 haplotype contribute to the risk of T2D in Tunisian subjects; no significant associations between CAPN10 diplotypes and T2D were demonstrated for Tunisians. PMID: 20470430
46. prostate cancer was positively associated with the CAPN10 rs3792267 G allele PMID: 20142250
47. The association with T2DM in different races was evaluated. SNP43-G allele, G/G genotype, 111/221 were risk factors to Mongoloid race. And SNP-C allele, 111/111 haplotype combination were risk factors to Caucasoid race, and SNP44-C allele to Hybrid race. PMID: 20193213
48. calpain-10 mRNA was elevated by 64% in pancreatic islets from patients with T2D compared with non-diabetic donors. Moreover, the calpain-10 expression correlated positively with arginine-stimulated insulin release in islets from non-diabetic donors PMID: 19688040
49. type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association PMID: 11704924
50. The variation of calpain-10 gene has impact on the variation of clinical metabolic parameter levels related to type 2 diabetes mellitus. PMID: 11774208
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相關疾病：

Diabetes mellitus, non-insulin-dependent, 1 (NIDDM1)
蛋白家族：

Peptidase C2 family
組織特異性：

Detected in primary skeletal muscle cells (at protein level). Ubiquitous.
數據庫鏈接：

HGNC: 1477

OMIM: 601283

KEGG: hsa:11132

STRING: 9606.ENSP00000375844

UniGene: Hs.728234

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