anti- FKBP1A antibody

Investigate the functions of FKBP1A with our Anti-FKBP1A Antibody, available in a 100µg vial. FKBP1A, a member of the FK506-binding protein family, plays a vital role in various cellular processes, including protein folding and immunosuppression. This highly specific antibody empowers researchers to explore the functions of FKBP1A with precision, contributing to a deeper understanding of its involvement in cellular homeostasis.

Key Features:

• Exceptional Specificity: Our Anti-FKBP1A Antibody is rigorously tested to ensure it accurately targets FKBP1A, minimizing the risk of cross-reactivity.
• Versatile Applications: Ideal for a wide range of experimental techniques, including immunohistochemistry, Western blotting, and immunoprecipitation.
• Ample Quantity: With 100µg, you have a generous supply for multiple experiments.
• Top-Tier Quality: Manufactured to the highest industry standards, guaranteeing consistent and reproducible results.
• Advance Your Research: Whether you're studying protein folding, immunosuppressive mechanisms, or other cellular functions, our Anti-FKBP1A Antibody is your key to unlocking new knowledge.

Investigate the intricate functions of FKBP1A with precision and elevate your research with our Anti-FKBP1A Antibody.

Product Name

FKBP1A antibody

Size

100µg

Form

liquid

Purification

Immunogen affinity purified

Purity

≥95% as determined by SDS-PAGE

Host

Rabbit

Clonality

polyclonal

Isotype

IgG

Storage

PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)

BACKGROUND

The protein encoded by this gene 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. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed.

IMMUNOGEN INFORMATION

Immunogen

FK506 binding protein 1A, 12kDa

Synonyms

FKBP1, FKBP12

Observed MW

12 kDa

APPLICATION

Tested Application

ELISA, IHC, WB

Recommended Dilution

WB: 1:500 - 1:2000; IHC: 1:50 - 1:200

UNIPROT INFORMATION

UniProt ID

P62942

IMAGES