50-168-2119
TCAP Mouse anti-Human, Clone: OTI11H10, liquid, TrueMAB™
Manufacturer: OriGene
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 50-168-2119-Each-of-1 | In Stock | ₹ 44,954.79 |
50-168-2119 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 44,954.79
GST (18%): ₹ 8,091.862
Total Price: ₹ 53,046.652
Antigen
TCAP
Classification
Monoclonal
Conjugate
Unconjugated
Gene
TCAP
Gene Alias
CMD1N, CMH25, LGMD2G, T-cap, TELE, telethonin
Host Species
Mouse
Purification Method
Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
8557
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Clone
OTI11H10
Formulation
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide
Gene Accession No.
O15273
Gene Symbols
TCAP
Immunogen
Full length human recombit protein of human TCAP produced in E.coli.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG1
Related Products
Description
- Sarcomere assembly is regulated by the muscle protein titin
- Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere
- It serves as a scaffold to which myofibrils and other muscle related proteins are attached
- TCAP is a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly
- Mutations in TCAP gene are associated with limb-girdle muscular dystrophy type 2G.Sarcomere assembly is regulated by the muscle protein titin
- Titin is a giant elastic protein with kinase activity that extends half the length of a sarcomere
- It serves as a scaffold to which myofibrils and other muscle related proteins are attached
- This gene encodes a protein found in striated and cardiac muscle that binds to the titin Z1-Z2 domains and is a substrate of titin kinase, interactions thought to be critical to sarcomere assembly
- Mutations in this gene are associated with limb-girdle muscular dystrophy type 2G.