GPATCH4 Antikörper (AA 236-262)

Produktnummer ABIN1538148

Dieses Anti-GPATCH4-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von GPATCH4 in WB. Geeignet für Human.

Kurzübersicht für GPATCH4 Antikörper (AA 236-262) (ABIN1538148)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GPATCH4 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: RB37527

Produktdetails anti-GPATCH4 Antikörper

Bindungsspezifität: AA 236-262

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

Immunogen: 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.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

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

Haltbarkeit: 6 months

Details zu GPATCH4

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

Andere Bezeichnung: GPATCH4

Hintergrund: 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.

Molekulargewicht: 50381

Gen-ID: 54865

UniProt: Q5T3I0