GPATCH4 anticorps (AA 236-262)

N° du produit ABIN1538148

Cet anticorps anti-GPATCH4 est un anticorps Lapin Polyclonal détectant GPATCH4 dans WB. Adapté pour Humain.

Aperçu rapide pour GPATCH4 anticorps (AA 236-262) (ABIN1538148)

Antigène: GPATCH4 (G Patch Domain Containing 4 (GPATCH4))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GPATCH4 est non-conjugé

Application: Western Blotting (WB)

Clone: RB37527

Détail du produit anti-GPATCH4 anticorps

Épitope: AA 236-262

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This GPATCH4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 236-262 amino acids from the Central region of human GPATCH4.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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.

Stock: 4 °C,-20 °C

Stockage commentaire: GPATCH4 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur GPATCH4

Antigène: GPATCH4 (G Patch Domain Containing 4 (GPATCH4))

Autre désignation: GPATCH4

Sujet: GPATCH4 (G patch domain-containing protein 4) is a 446 amino acid protein containing one G-patch domain. Existing as three alternatively spliced isoforms, the gene encoding GPATCH4 maps to human chromosome 1q23.1 and mouse chromosome 3 F1. Spanning around 260 million base pairs, chromosome 1 is the largest human chromosome and comprises 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Poids moléculaire: 50381

ID gène: 54865

UniProt: Q5T3I0