• Target：
• Troponin I-FS

• Gene Name：
• TNNI2

• Protein Name：
• Troponin I fast skeletal muscle

• Human Gene Id：
• 7136

• Human Swiss Prot No：
• P48788

• Mouse Swiss Prot No：
• P13412

• Immunogen：
• Purified recombinant fragment of human Troponin I-FS expressed in E. Coli.

• Specificity：
• Troponin I-FS Monoclonal Antibody detects endogenous levels of Troponin I-FS protein.

• Formulation：
• Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• Source：
• Monoclonal, Mouse

• Dilution：
• WB 1:500 - 1:2000. IHC 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000.. IF 1:50-200

• Purification：
• Affinity purification

• Storage Stability：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• Other Name：
• TNNI2;Troponin I; fast skeletal muscle;Troponin I, fast-twitch isoform

• Molecular Weight(Da)：
• 21kD

• References：
• 1. Am J Hum Genet. 2009 Nov;85(5):628-42.
  2. Cell Motil Cytoskeleton. 2008 Aug;65(8):652-61.

• Background：
• This gene encodes a fast-twitch skeletal muscle protein, a member of the troponin I gene family, and a component of the troponin complex including troponin T, troponin C and troponin I subunits. The troponin complex, along with tropomyosin, is responsible for the calcium-dependent regulation of striated muscle contraction. Mouse studies show that this component is also present in vascular smooth muscle and may play a role in regulation of smooth muscle function. In addition to muscle tissues, this protein is found in corneal epithelium, cartilage where it is an inhibitor of angiogenesis to inhibit tumor growth and metastasis, and mammary gland where it functions as a co-activator of estrogen receptor-related receptor alpha. This protein also suppresses tumor growth in human ovarian carcinoma. Mutations in this gene cause myopathy and distal arthrogryposis type 2B. Alternatively spliced trans

• Function：
• caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease:Defects in TNNI2 are a cause of distal arthrogryposis type 2B (DA2B) [MIM:601680]; 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.,function:Troponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.,similarity:Belongs to the troponin I family.,subunit:Binds to actin and tropomyosin.,

• Subcellular Location：
• nucleus,cytosol,troponin complex,

• Expression：
• Muscle,Skeletal muscle,

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