FASTKD5 anticorps (AA 501-600) (Biotin)

N° du produit ABIN896871

Cet anticorps anti-FASTKD5 est un anticorps Lapin Polyclonal détectant FASTKD5 dans ELISA, IHC (p) et IHC (fro). Adapté pour Humain.

Aperçu rapide pour FASTKD5 anticorps (AA 501-600) (Biotin) (ABIN896871)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

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

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

Détail du produit anti-FASTKD5 anticorps (Biotin)

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

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 for 12 months.

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