FASTKD5 anticorps (AA 501-600) (FITC)

N° du produit ABIN896866

Cet anticorps Lapin Polyclonal détecte spécifiquement FASTKD5 dans IF (cc) et IF (p). Il présente une réactivité envers Humain.

Aperçu rapide pour FASTKD5 anticorps (AA 501-600) (FITC) (ABIN896866)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FASTKD5 est conjugé à/à la FITC

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

Détail du produit anti-FASTKD5 anticorps (FITC)

Épitope: AA 501-600

Réactivité croisée: Humain

Homologie: Mouse,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from mouse FASTKD5

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

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

Date de péremption: 12 months

Détails sur FASTKD5

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

Autre désignation: FASTKD5

Sujet:

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.

ID gène: 380601

UniProt: Q7TMV3

Pathways: SARS-CoV-2 Protein Interactome