TM9SF4 anticorps (AA 101-200) (Biotin)

N° du produit ABIN1398469

Cet anticorps Lapin Polyclonal détecte spécifiquement TM9SF4 dans WB, IHC (p), ELISA et IHC (fro). Il présente une réactivité envers Souris.

Aperçu rapide pour TM9SF4 anticorps (AA 101-200) (Biotin) (ABIN1398469)

Antigène: TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TM9SF4 est conjugé à/à la Biotin

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

Détail du produit anti-TM9SF4 anticorps (Biotin)

Épitope: AA 101-200

Réactivité croisée: Souris

Homologie: Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human TM9SF4

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
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 TM9SF4

Antigène: TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))

Autre désignation: TM9SF4

Sujet:

Synonyms: dJ836N17.2, Transmembrane 9 superfamily member 4, TM9SF4, KIAA0255

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: 9777

UniProt: Q92544