|Application ||WB, E|
|Other Accession||P27768, P02643, P13412, NP_003273.1, NP_001139301.1|
|Predicted||Mouse, Rabbit, Rat|
|Calculated MW||21339 Da|
|Antigen Region||1-30 aa|
|Other Names||Troponin I, fast skeletal muscle, Troponin I, fast-twitch isoform, TNNI2|
|Target/Specificity||This TNNI2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human TNNI2.|
|Format||Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.|
|Storage||Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||TNNI2 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Troponin I is the inhibitory subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity.|
email@example.com, and receive a free "I Love Antibodies" mug.
Provided below are standard protocols that you may find useful for product applications.
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 transcript variants have been found for this gene. [provided by RefSeq].
Bailey, S.D., et al. Diabetes Care (2010) In press :
Talmud, P.J., et al. Am. J. Hum. Genet. 85(5):628-642(2009)
Perez-Ilzarbe, M., et al. Eur. J. Heart Fail. 10(11):1065-1072(2008)
Moran, C.M., et al. Cell Motil. Cytoskeleton 65(8):652-661(2008)
Li, Y., et al. Biochem. Biophys. Res. Commun. 369(4):1034-1040(2008)
If you have any additional inquiries please email technical services at firstname.lastname@example.org.