Cardiac Troponin T (TNNT2) Mouse Monoclonal Antibody [Clone ID: UMAB205]

CAT#: UM870097

Troponin T (TNNT2) mouse monoclonal antibody,clone UMAB205

Size: 30 ul 100 ul



  View other "UMAB205" antibodies (2)

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【特别福利】购一抗正装产品,免费领10ul抗体试用装

CNY 1,150.00


货期*
现货

规格
    • 30 ul

Product images

经常一起买 (4)
Transient overexpression lysate of troponin T type 2 (cardiac) (TNNT2), transcript variant 1
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Recombinant protein of human troponin T type 2 (cardiac) (TNNT2), transcript variant 1, 20 µg
    • 20 ug

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Recombinant protein of human troponin T type 2 (cardiac) (TNNT2), transcript variant 1, 100 µg
    • 100 ug

CNY 9,998.00

Specifications

Product Data
Clone Name UMAB205
Applications 10k-ChIP, IHC, WB
Recommend Dilution IHC 1:100~200
Reactivity Human, Mouse, Rat
Host Mouse
Clonality Monoclonal
Immunogen Full length human recombinant protein of human TNNT2 (NP_000355) produced in E.coli.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Concentration 0.5~1.0 mg/ml (Lot Dependent)
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Unconjugated
Storage Condition Store at -20°C as received.
Predicted Protein Size 35.4 kDa
Gene Name troponin T2, cardiac type
Background The protein encoded by this gene is the tropomyosin-binding subunit of the troponin complex, which is located on the thin filament of striated muscles and regulates muscle contraction in response to alterations in intracellular calcium ion concentration. Mutations in this gene have been associated with familial hypertrophic cardiomyopathy as well as with dilated cardiomyopathy. Transcripts for this gene undergo alternative splicing that results in many tissue-specific isoforms, however, the full-length nature of some of these variants has not yet been determined. (provided by RefSeq, Jul 2008)
Synonyms CMD1D; CMH2; CMPD2; cTnT; LVNC6; RCM3; TnTC
Reference Data
Protein Families Druggable Genome
Protein Pathways Cardiac muscle contraction, Dilated cardiomyopathy, Hypertrophic cardiomyopathy (HCM)
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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