FKBP10 antibody (AA 29-532)

Catalog No. ABIN7601140

The Rabbit Polyclonal anti-FKBP10 antibody has been validated for WB, ELISA, FACS, ICC and IF. It is suitable to detect FKBP10 in samples from Human.

Quick Overview for FKBP10 antibody (AA 29-532) (ABIN7601140)

Target: FKBP10 (FK506 Binding Protein 10, 65 KDa (FKBP10))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FKBP10 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunocytochemistry (ICC), Immunofluorescence (IF)

Product Details anti-FKBP10 Antibody

Binding Specificity: AA 29-532

Purpose: Anti-FKBP10 Antibody Picoband®

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Characteristics: Anti-FKBP10 Antibody Picoband® (ABIN7601140). Tested in ELISA, Flow Cytometry, IF, ICC, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human FKBP10 recombinant protein (Position: R29-E532).

Isotype: IgG

Application Details

Application Notes: Western blot, 0.1-0.25 μg/mL, Human
Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/mL, -
1. Alanay, Y., Avaygan, H., Camacho, N., Utine, G. E., Boduroglu, K., Aktas, D., Alikasifoglu, M., Tuncbilek, E., Orhan, D., Bakar, F. T., Zabel, B., Superti-Furga, A., and 12 others. Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta. Am. J. Hum. Genet. 86: 551-559, 2010. Note: Erratum: Am. J. Hum. Genet. 87: 572-573, 2010. 2. Alanay, Y., Krakow, D. Response to Shaheen et al. (Letter) Am. J. Hum. Genet. 87: 308 only, 2010. 3. Bank, R. A., Robins, S. P., Wijmenga, C., Breslau-Siderius, L. J., Bardoel, A. F. J., Van der Sluijs, H. A., Pruijs, H. E. H., TeKoppele, J. M. Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17. Proc. Nat. Acad. Sci. 96: 1054-1058, 1999.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Target Details for FKBP10

Target: FKBP10 (FK506 Binding Protein 10, 65 KDa (FKBP10))

Alternative Name: FKBP10

Background:

Synonyms: Histone deacetylase 10, HD10, HDAC10

Tissue Specificity: Ubiquitous. High expression in liver, spleen, pancreas and kidney.

Background: FK506-binding protein 10 is a protein that in humans is encoded by the FKBP10 gene. The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. This protein localizes to the endoplasmic reticulum and acts as a molecular chaperone. Alternatively spliced variants encoding different isoforms have been reported, but their biological validity has not been determined.

Molecular Weight: 72 kDa

Gene ID: 60681

Pathways: SARS-CoV-2 Protein Interactome