Thermo Fisher Scientific TNNT1 Polyclonal Antibody
Human TNNT1 단백질을 인식하는 Rabbit Polyclonal Antibody로, IHC(P)에서 1:500~1:1,000 희석 비율로 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol 완충액에 보존. 근육 수축 조절 단백질 연구에 적합.
- 판매단위
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Applications
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:500–1:1,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human TNNT1. Recombinant protein control fragment (Product #RP-103332) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.07 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7.2, with 40% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2791533 |
Product Specific Information
Immunogen sequence:
EEEEAPEEPE PVAEPEEERP KPSRPVVPPL IPPKIPEGE
Target Information
This gene encodes a protein that is a subunit of troponin, a regulatory complex located on the thin filament of the sarcomere.
Troponin regulates striated muscle contraction in response to changes in intracellular calcium concentration and is composed of three subunits:
- Troponin C: binds calcium
- Troponin T: binds tropomyosin
- Troponin I: inhibitory subunit
TNNT1 encodes the slow skeletal troponin T subunit.
Mutations in this gene cause nemaline myopathy type 5 (Amish nemaline myopathy), a neuromuscular disorder characterized by muscle weakness and rod-shaped inclusions in skeletal muscle fibers.
Affected infants often die due to respiratory insufficiency, typically within the second year.
Multiple transcript variants encoding different isoforms have been identified for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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