TGM1 anticorps

N° du produit ABIN5699641

Cet anticorps Lapin Polyclonal détecte spécifiquement TGM1 dans WB, IHC, IP et ELISA. Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour TGM1 anticorps (ABIN5699641)

Antigène: TGM1 (Transglutaminase 1, Keratinocyte (TGM1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TGM1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunoprecipitation (IP), ELISA

Détail du produit anti-TGM1 anticorps

Fonction: TGM1 antibody

Immunogène: transglutaminase 1 (K polypeptide epidermal type I, protein-glutamine-gamma-glutamyltransferase)

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

mouse kidney tissue were subjected to SDS PAGE followed by western blot with FNab08649(TGM1 antibody) at dilution of 1:500

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

Agent conservateur: Sodium azide

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

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur TGM1

Antigène: TGM1 (Transglutaminase 1, Keratinocyte (TGM1))

Autre désignation: TGM1

Sujet:

Synonyms: Protein-glutamine gamma-glutamyltransferase K|Epidermal TGase|Transglutaminase K (TG(K), TGK, TGase K)|Transglutaminase-1 (TGase-1)|TGM1|KTG

Background: The protein encoded by this gene is a membrane protein that catalyzes the addition of an alkyl group from an akylamine to a glutamine residue of a protein, forming an alkylglutamine in the protein. This protein alkylation leads to crosslinking of proteins and catenation of polyamines to proteins. This gene contains either one or two copies of a 22 nt repeat unit in its 3' UTR. Mutations in this gene have been associated with autosomal recessive lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE).

ID gène: 7051

UniProt: P22735