FKBP12 Monoclonal Antibody (OTI3B3), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA524953-Each-of-1 | In Stock | ₹ 54,201.00 |
PIMA524953 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 54,201.00
GST (18%): ₹ 9,756.18
Total Price: ₹ 63,957.18
Antigen
FKBP12
Classification
Monoclonal
Concentration
1.0 mg/mL
Formulation
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3
Gene Accession No.
P62942
Gene Symbols
FKBP1A
Immunogen
Full length human recombinant protein of FKBP1A produced in HEK293T cell
Quantity
100μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG2b
Applications
Flow Cytometry, Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Clone
OTI3B3
Conjugate
Unconjugated
Gene
FKBP1A
Gene Alias
12 kDa FK506-binding protein; 12 kDa FKBP; calstabin 1; calstabin-1; EC 5.2.1.8; FK506 binding protein 1a; FK506 binding protein 1A, 12kDa; FK506 binding protein 2 (13 kDa); FK506 binding protein12; FK506-binding protein 1; FK506-binding protein 1 (12kD); FK506-binding protein 12; FK506-binding protein 1a; FK506-binding protein 1A (12kD); FK506-binding protein, T-cell, 12-kD; Fkbp; FKBP1; FKBP12; FKBP-12; FKBP12-Exip3; Fkbp1a; FKBP-1A; Fkbp2; Immunophilin FKBP12; peptidyl-prolyl cis-trans isomerase FKBP1A; PKC12; PKCI2; PPIASE; PPIase FKBP1A; protein kinase C inhibitor 2; rotamase
Host Species
Mouse
Purification Method
Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
2280
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Related Products
Description
- FKBP12 is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking
- The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin
- It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor
- It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor
- In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium.