CAPN10 Antibody

Code CSB-PA864027LA01HU
Size US$166
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  • Immunofluorescence staining of U251 cells with CSB-PA864027LA01HU at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) CAPN10 Polyclonal antibody
Uniprot No.
Target Names
CAPN10
Alternative Names
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
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Calpain-10 protein (1-287AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The CAPN10 Antibody (Product code: CSB-PA864027LA01HU) is Non-conjugated. For CAPN10 Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA864027LB01HU CAPN10 Antibody, HRP conjugated ELISA
FITC CSB-PA864027LC01HU CAPN10 Antibody, FITC conjugated
Biotin CSB-PA864027LD01HU CAPN10 Antibody, Biotin conjugated ELISA
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, IF
Recommended Dilution
Application Recommended Dilution
IF 1:50-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
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.

Customer Reviews and Q&A

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Target Background

Function
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.
Gene References into Functions
  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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Involvement in disease
Diabetes mellitus, non-insulin-dependent, 1 (NIDDM1)
Protein Families
Peptidase C2 family
Tissue Specificity
Detected in primary skeletal muscle cells (at protein level). Ubiquitous.
Database Links

HGNC: 1477

OMIM: 601283

KEGG: hsa:11132

STRING: 9606.ENSP00000375844

UniGene: Hs.728234

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