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Rabbit Anti-Troponin T fast + slow skeletal muscle/FITC Conjugated antibody
Function:
Troponin T is the tropomyosin-binding subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.
Tissue Specificity:
In fetal and adult fast skeletal muscles, with a higher level expression in fetal than in adult muscle.
DISEASE:
Defects in TNNT3 are a cause of distal arthrogryposis type 2B (DA2B) [MIM:60336]; also known as arthrogryposis multiplex congenita, distal, type 2B (AMCD2B). DA2B is a form of inherited multiple congenital contractures. Affected individuals have vertical talus, ulnar deviation in the hands, severe camptodactyly, and a distinctive face characterized by a triangular shape, prominent nasolabial folds, small mouth and a prominent chin.
Similarity:
Belongs to the troponin T family.
Database links:
Entrez Gene: 7140 Human
Entrez Gene: 21957 Mouse
Entrez Gene: 24838 Rat
Omim: 600692 Human
SwissProt: P45378 Human
SwissProt: Q9QZ47 Mouse
SwissProt: P09739 Rat
Unigene: 73454 Human
Unigene: 389992 Mouse
Unigene: 15488 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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