Rabbit Anti-Troponin I fast + slow skeletal muscle antibody

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AMCD2B; DA2B; DKFZp451O223; Fast twitch skeletal muscle troponin I; FSSV; fsTnI; OTTHUMP00000014141; OTTHUMP00000014142; OTTHUMP00000014143; OTTHUMP00000033877; OTTHUMP00000033909; OTTHUMP00000033910; SSTNI; TNN1; Troponin I fast twitch 2; Troponin I type

Cat:

SL10617R

Species Reactivity：

(predicted: Human,Chicken,Pig,Cow,Rabbit,Sheep,)

Immunogen：

KLH conjugated synthetic peptide derived from human TNNI1+TNNI2 :51-150/182

Format：

Liquid

Storage instructions：

Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

Concentration：

1mg/ml

Clonality：

Polyclonal

Isotype：

IgG

Applications：

WB=1:500-2000ELISA=1:5000-10000IHC-P=1:100-500IHC-F=1:100-500ICC=1:100-500IF=1:100-500（Paraffin sections need to do antigen repair）not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.

Host：

Rabbit

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Unit:

Price: $228.00

Product PDFs

Datasheet: Down Datasheet

Other Information
Citations
Protein Attributes
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Troponin proteins associate with tropomyosin and regulate the calcium sensitivity of the myofibril contractile apparatus of striated muscles. Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. The TnI-fast and TnI-slow genes are expressed in fast-twitch and slow-twitch skeletal muscle fibers, respectively, while the TnI-cardiac gene is expressed exclusively in cardiac muscle tissue.

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.

Subunit:
Binds to actin and tropomyosin.

DISEASE:
Arthrogryposis, distal, 2B (DA2B) [MIM:60336]: 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.

Similarity:
Belongs to the troponin I family.

SWISS:
P19237

Gene ID:
7135

Database links:

Entrez Gene: 7135 Human

Entrez Gene: 7136 Human

Omim: 191042 Human

Omim: 191043 Human

SwissProt: P19237 Human

SwissProt: P48788 Human

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