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Mouse Monoclonal Troponin I-FS antibody [2F12A8] (STJ98435)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IHC, FC, ELISA
Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for Troponin I-FS Monoclonal Antibody.
Check alternative names for the antibodyExpand
TNNI2 antibody,|AMCD 2B antibody|AMCD2B antibody|DA 2B antibody|DA2B antibody|fast skeletal muscle antibody|Fast twitch skeletal muscle troponin I antibody|fast-twitch isoform antibody|FSSV antibody|fsTnI antibody|TNNI 2 antibody|Tnni2 antibody|TNNI2_HUMAN antibody|tro antibody|Troponin I antibody|Troponin I fast skeletal muscle antibody|Troponin I fast twitch 2 antibody|Troponin I fast twitch isoform antibody|Troponin I fast twitch skeletal muscle isoform antibody|Troponin I skeletal fast antibody|Troponin I type 2 (skeletal fast) antibody|Troponin I type 2 antibody|Anti-Troponin I fast skeletal muscle antibody (ab97711)
SCBT cat No: To be updated
Troponin I-FS Monoclonal Antibody
|Catalogue No.|| |
Troponin I-FS Monoclonal Antibody detects endogenous levels of Troponin I-FS protein.
Purified recombinant fragment of human Troponin I-FS expressed in E Coli
WB, IHC, FC, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; IHC 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000
Troponin I-FS Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
Troponin I-FS Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Troponin I, fast skeletal muscle antibody, Troponin I, fast-twitch isoform antibody
|Protein names|| |
Troponin I, fast skeletal muscle , Troponin I, fast-twitch isoform
|Protein function|| |
Troponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.
|Involvement in disease|| |
Arthrogryposis, distal, 2B (DA2B) [MIM:601680]: A form of distal arthrogryposis, a disease characterized by congenital joint contractures that mainly involve two or more distal parts of the limbs, in the absence of a primary neurological or muscle disease. DA2B is characterized by contractures of the hands and feet, and a distinctive face characterized by prominent nasolabial folds, small mouth and downslanting palpebral fissures. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the troponin I family.
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St John’s Laboratory Ltd.
|Product type|| |
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