Application: IHC
Clonality: Polyclonal
Host: Rabbit
Reactivity: Human
Protein Description: troponin T type 1 (skeletal, slow)
Gene Name: TNNT1
Alternative Gene Name: ANM, FLJ98147, MGC104241, NEM5, STNT, TNT, TNTS
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000064179: 97%, ENSRNOG00000028041: 95%
Entrez Gene ID: 7138
Uniprot ID: P13805
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
Clonality: Polyclonal
Host: Rabbit
Reactivity: Human
Protein Description: troponin T type 1 (skeletal, slow)
Gene Name: TNNT1
Alternative Gene Name: ANM, FLJ98147, MGC104241, NEM5, STNT, TNT, TNTS
Isotype: IgG
Interspecies mouse/rat: ENSMUSG00000064179: 97%, ENSRNOG00000028041: 95%
Entrez Gene ID: 7138
Uniprot ID: P13805
Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
Storage Temperature: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
| Cognate Antibody/Antigen for Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) | |
| Antigen | PrEST Antigen TNNT1 (ATL-APrEST87837) |
| Documents & Links for Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) | |
| Datasheet | Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) at Atlas |
| Documents & Links for Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) | |
| Datasheet | Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) Datasheet (External Link) |
| Vendor Page | Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) |
| Citations for Anti TNNT1 pAb (ATL-HPA058448 w/enhanced validation) – 2 Found |
| Human MuStem Cell Grafting into Infarcted Rat Heart Attenuates Adverse Tissue Remodeling and Preserves Cardiac Function. Mol Ther Methods Clin Dev. 2020 Jun 15;18:446-463. doi: 10.1016/j.omtm.2020.06.009. eCollection 2020 Sep 11. PubMed |
| Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy. Acta Neuropathol Commun. 2020 Aug 20;8(1):142. doi: 10.1186/s40478-020-01017-1. PubMed |