FKBP1A antibody (AA 43-74)

Catalog No. ABIN3030968

The Rabbit Polyclonal anti-FKBP1A antibody has been validated for WB, IHC and ELISA. It is suitable to detect FKBP1A in samples from Human.

Quick Overview for FKBP1A antibody (AA 43-74) (ABIN3030968)

Target: FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FKBP1A antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Product Details anti-FKBP1A Antibody

Binding Specificity: AA 43-74

Cross-Reactivity (Details): Expected species reactivity: Mouse, Rat, Bovine, Rabbit

Purification: Purified

Immunogen: A portion of amino acids 43-74 from the human protein was used as the immunogen for this FKBP12 antibody.

Isotype: Ig Fraction

Application Details

Application Notes: Titration of the FKBP12 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:10-1:50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Aliquot the FKBP12 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Target Details for FKBP1A

Target: FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))

Alternative Name: FKBP12

Background: 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.

UniProt: P62942

Pathways: Negative Regulation of Transporter Activity, Methionine Biosynthetic Process