FASTKD5 antibody (AA 501-600) (AbBy Fluor® 750)

Catalog No. ABIN5002486

The Rabbit Polyclonal anti-FASTKD5 antibody has been validated for IF (cc) and IF (p). It is suitable to detect FASTKD5 in samples from Human.

Quick Overview for FASTKD5 antibody (AA 501-600) (AbBy Fluor® 750) (ABIN5002486)

Target: FASTKD5 (FAST Kinase Domains 5 (FASTKD5))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FASTKD5 antibody is conjugated to AbBy Fluor® 750

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-FASTKD5 Antibody (AbBy Fluor® 750)

Binding Specificity: AA 501-600

Cross-Reactivity: Human

Predicted Reactivity: Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from mouse FASTKD5

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for FASTKD5

Target: FASTKD5 (FAST Kinase Domains 5 (FASTKD5))

Alternative Name: FASTKD5

Background:

Synonyms: C78212, mKIAA1792, FAST kinase domain-containing protein 5, Fastkd5, Kiaa1792

Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis which are thought important for seminal production and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20.

Gene ID: 380601

UniProt: Q7TMV3

Pathways: SARS-CoV-2 Protein Interactome