Troponin T, Slow Skeletal Muscle (TNNI1) ELISA试剂盒

TNNI1 encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. 再加上,我们可以发TNNI1 抗体 (61)TNNI1 蛋白 (14)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
TNNI1 7138 P13805
TNNI1 21955 O88346
TNNI1 171409 Q7TNB2
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Showing 8 out of 47 products:

产品编号 适用 灵敏度 范围 图像 规格 供应商 交付 价格 详细
5.5 pg/mL 15.6 pg/mL - 1000 pg/mL 96 Tests Log in to see 13至16个工作日
Pig 7.8 pg/mL 31.25-2000 pg/mL Typical standard curve 96 Tests Log in to see 15至18个工作日
小鼠 5.8 pg/mL 15.62 pg/mL - 1000 pg/mL 96 Tests Log in to see 13至16个工作日
大鼠 5.2 pg/mL 15.62 pg/mL - 1000 pg/mL 96 Tests Log in to see 13至16个工作日
Cow 3.13 pg/mL n/a   96 Tests Log in to see 15至18个工作日
小鸡 37.5 pg/mL 62.5-4000 pg/mL   96 Tests Log in to see 12至14个工作日
0.094 ng/mL 0.156-10 ng/mL   96 Tests Log in to see 12至14个工作日
9.375 pg/mL 15.625-1000 pg/mL   96 Tests Log in to see 12至14个工作日

引用最多的TNNI1 ELISA试剂盒

  1. Human TNNI1 ELISA Kit for Sandwich ELISA - ABIN418922 : King, Abreu, Cheng, Chertoff, Brotto, Kelly, Brotto: A multimodal assessment of balance in elderly and young adults. in Oncotarget 2016 (PubMed)

适于 TNNI1 相互作用对的更多 ELISA 试剂盒

Human Troponin T, Slow Skeletal Muscle (TNNI1) interaction partners

  1. High TNNT1 expression is associated with breast cancer.

  2. This study describes the first TNNT1 mutation that transmits in an autosomal dominant fashion to cause nemaline myopathy.

  3. investigated the effects of one of these mutations, K247R of TnT, on the picosecond dynamics of the Tn core domain (Tn-CD), consisting of TnC, TnI and TnT2 (183-288 residues of TnT), by carrying out the quasielastic neutron scattering measurements on the reconstituted Tn-CD containing either the wild-type TnT2 (wtTn-CD) or the mutant TnT2 (K247R-Tn-CD) in the absence and presence of Ca(2+)

  4. Data suggest that mutations in troponin C (TnC, A8V) and troponin T (TnT, delta14-TnT) found in patients with hypertrophic cardiomyopathy together fully stabilize the active M state of regulated actin (the actin-tropomyosin-troponin complex).

  5. pathogenesis of TNNT1 myopathies

  6. Copeptin and troponin T measurement could potentially improve the prehospital diagnostic and prognostic classification of patients with a suspected AMI.

  7. TNNT1 genetic and epigenetic variations are associated with HDL-C levels and coronary artery disease.

  8. Three homologous genes have evolved in vertebrates to encode three muscle type-specific TnT isoforms: TNNT1 for slow skeletal muscle TnT, TNNT2 for cardiac muscle TnT, and TNNT3 for fast skeletal muscle TnT.

  9. Nemaline body myopathy Palestinian patients were found to have a novel mutation in troponin T1.

  10. troponin T and creatinine kinase isoenzyme (CK-MB) have roles in combined renal and myocardial injuries in asphyxiated infants

  11. Biopsy-proven acute and viral myocarditis is associated with elevated concentrations of hs-TnT.

  12. Troponin T1 blood levels had a positive association with increased risk for hypertrophic cardiomyopathy.

  13. TNNT1 DNA methylation levels were positively correlated with mean HDL particle size, HDL-phospholipid, HDL-apolipoprotein AI, HDL-C and TNNT1 expression levels.

  14. Human slow skeletal troponin T (HSSTnT) isoforms, despite being homologues of cardiac TnT may display distinct functional properties in muscle regulation.

  15. analysis of parameters of oxygen-dependent metabolism of neutrophils by NBT test and levels of vWF antigen in the serum can be used for predicting the risk of unfavorable outcome in patients with ACS and normal troponin T

  16. In heart failure patients with normal ejection fraction, highly sensitive troponin T and heart fatty acid binding protein are elevated independent of coronary artery disease.

  17. baseline cTnT levels are higher in patients with MPI evidence of reversible myocardial ischaemia than those without reversible ischaemia

  18. carotid-femoral pulse wave and office pulse pressure are associated with minimally elevated hsTnT levels in the elderly

  19. the hypertrophic phenotype associated with the TnT mutations can be characterized by a significant increase in disorder of rigor cross-bridges.

  20. Elevated serum troponin T levels are associated with different conditions related to the severity of hypertrophic cardiomyopathy.

Mouse (Murine) Troponin T, Slow Skeletal Muscle (TNNI1) interaction partners

  1. Mouse tumor endothelial cells express troponin T.

  2. demonstrated that ssTnT deficiency resulted in significantly decreased levels of other slow fibre-specific myofilament proteins whereas fast fibre-specific myofilament proteins were increased correspondingly

  3. the induction of Tnnt1 gene expression in adult mouse brains by ketamine may illustrate the genes involved in the metabolic syndromes observed in neuropsychiatric disorders

  4. Data show that cardiac expression of slow skeletal troponin T (Tnnt1) strictly depends on the physical interaction between GATA4-FOG2 in the myocardium of both atria and ventricles.

TNNI1 抗原简介

Antigen Summary

This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with TNNI1

  • troponin T1, slow skeletal type (TNNT1) 抗体
  • troponin I, slow skeletal muscle (tnni1) 抗体
  • troponin I1, slow skeletal type (TNNI1) 抗体
  • troponin I type 1 (skeletal, slow) (tnni1) 抗体
  • troponin T1, skeletal, slow (Tnnt1) 抗体
  • troponin T1, slow skeletal type (Tnnt1) 抗体
  • troponin T1, slow skeletal type S homeolog (tnnt1.S) 抗体
  • troponin T type 1 (skeletal, slow) (tnnt1) 抗体
  • ANM 抗体
  • AW146156 抗体
  • Fang2 抗体
  • MGC75706 抗体
  • NEM5 抗体
  • ssTnT 抗体
  • sTnT 抗体
  • TNNI1 抗体
  • Tnnt 抗体
  • Tnt 抗体
  • tnTs 抗体
  • zgc:193831 抗体
  • zgc:193865 抗体

Protein level used designations for TNNI1

nemaline myopathy type 5 , slow skeletal muscle troponin T , troponin T, slow skeletal muscle , troponin-T1, skeletal, slow , troponin I, skeletal, slow , troponin I type 1 (skeletal, slow) , troponin I, skeletal, slow 1 , sTnT , tnTs , troponin T1, skeletal, slow , troponin T slow type isoform sTnT1 , skeletal muscle slow-twitch TnT

7138 Homo sapiens
100196284 Salmo salar
469636 Pan troglodytes
394556 Xenopus (Silurana) tropicalis
282095 Bos taurus
396579 Sus scrofa
21955 Mus musculus
171409 Rattus norvegicus
444636 Xenopus laevis
558627 Danio rerio
100720501 Cavia porcellus
476383 Canis lupus familiaris
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