Coagulation Factor IX antibody

Catalog No. ABIN7258664

Product Details anti-Coagulation Factor IX Antibody

Target: Coagulation Factor IX (F9)

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Coagulation Factor IX antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human Factor IX / F9 (NP_000124.1).

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:2000 IF 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Coagulation Factor IX

Target: Coagulation Factor IX (F9)

Alternative Name: Factor IX / F9 (F9 Products)

Synonyms: AA407498 antibody, AI506714 antibody, AK-3 antibody, Ak3l antibody, Ak3l1 antibody, Akl3l antibody, FIX antibody, HEMB antibody, P19 antibody, PTC antibody, THPH8 antibody, AW111646 antibody, Cf-9 antibody, Cf9 antibody, f9 antibody, zgc:109775 antibody, fix antibody, ptc antibody, hemb antibody, FIXA antibody, zgc:136807 antibody, adenylate kinase 3 antibody, coagulation factor IX antibody, coagulation factor IXa antibody, coagulation factor 9 antibody, coagulation factor 9 S homeolog antibody, Coagulation factor IX antibody, coagulation factor IXb antibody, Ak3 antibody, F9 antibody, f9a antibody, f9 antibody, CpipJ_CPIJ003776 antibody, CpipJ_CPIJ009129 antibody, CpipJ_CPIJ013063 antibody, CpipJ_CPIJ013624 antibody, Tsp_01441 antibody, f9.S antibody, fa9 antibody, f9b antibody

Background: 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. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.

Molecular Weight:

Observed_MW: 50 kDa

Calculated_MW: 47 kDa/51 kDa

Gene ID: 2158

UniProt: P00740