Anti-TCAP Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-TCAP Antibody (CSB-PA023264ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Telethonin Antibody,Titin cap protein Antibody,TCAP Antibody

More alternative names for the antibody
19 kDa sarcomeric protein antibody|CMD1N antibody|CMH25 antibody|LGMD2G antibody|Limb girdle muscular dystrophy 2G (autosomal recessive) antibody|T-cap antibody|Tcap antibody|TELE antibody|Telethonin antibody|TELT_HUMAN antibody|Titin cap protein antibody|Titin-cap antibody
Anti-Telethonin antibody [EPR8375] (ab133646)
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Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-TCAP Antibody

Catalogue No.

CSB-PA023264ESR1HU

Reactivity

Human

Immunogen

Recombinant human Telethonin protein (1-167AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

19 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:8557( Human), Entrez Gene:21393( Mouse), Entrez Gene:688173( Rat), Omim:604488( Human), SwissProt:O15273( Human), SwissProt:O70548( Mouse), Unigene:77628( Human), Unigene:10762( Mouse)

Protein function

Muscle assembly regulating factor. Mediates the antiparallel assembly of titin (TTN) molecules at the sarcomeric Z-disk.

Protein tissue specificity

Heart and skeletal muscle.

Involvement in disease

Cardiomyopathy, familial hypertrophic 25 (CMH25) [MIM:607487]: A hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Limb-girdle muscular dystrophy 2G (LGMD2G) [MIM:601954]: An autosomal recessive degenerative myopathy characterized by proximal and distal muscle weakness and atrophy in the limbs, dystrophic changes on muscle biopsy, and absence of telethonin. Cardiac muscle is involved in a subset of patients. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein cellular localization

Cytoplasm, myofibril, sarcomere .

Research area

All research areas>Structural Proteins>Telethonin
(View all antibody categories related to Structural Proteins)

Note

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Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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