Coagulation Factor IX Antikörper (AA 266-295)

Produktnummer ABIN1538212

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch Coagulation Factor IX in WB. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für Coagulation Factor IX Antikörper (AA 266-295) (ABIN1538212)

Target: Coagulation Factor IX (F9)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Coagulation Factor IX Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: RB36658

Produktdetails anti-Coagulation Factor IX Antikörper

Bindungsspezifität: AA 266-295

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

Immunogen: This F9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 266-295 amino acids from the Central region of human F9.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:2000. 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: F9 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 Coagulation Factor IX

Target: Coagulation Factor IX (F9)

Andere Bezeichnung: F9

Hintergrund: This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease.

Molekulargewicht: 51778

Gen-ID: 2158

NCBI Accession: NP_000124

UniProt: P00740