FASTKD5 antibody (AA 501-600) (Biotin)

Catalog No. ABIN896871

Product Details anti-FASTKD5 Antibody (Biotin)

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

Binding Specificity: AA 501-600

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FASTKD5 antibody is conjugated to Biotin

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

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: IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Expiry Date: 12 months

Target Details for FASTKD5

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

Alternative Name: FASTKD5 (FASTKD5 Products)

Synonyms: dJ1187M17.5 antibody, C78212 antibody, mKIAA1792 antibody, Fastkd5-ps1 antibody, RGD1563839 antibody, FAST kinase domains 5 antibody, U-box domain containing 5 antibody, FASTKD5 antibody, UBOX5 antibody, Fastkd5 antibody

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