Fibrinogen beta Chain anticorps (AA 202-491)

N° du produit ABIN3021950

Détail du produit anti-Fibrinogen beta Chain anticorps

Antigène: Fibrinogen beta Chain (FGB)

Épitope: AA 202-491

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Fibrinogen beta Chain est non-conjugé

Application: Western Blotting (WB)

Séquence: LENLRSKIQK LESDVSAQME YCRTPCTVSC NIPVVSGKEC EEIIRKGGET SEMYLIQPDS SVKPYRVYCD MNTENGGWTV IQNRQDGSVD FGRKWDPYKQ GFGNVATNTD GKNYCGLPGE YWLGNDKISQ LTRMGPTELL IEMEDWKGDK VKAHYGGFTV QNEANKYQIS VNKYRGTAGN ALMDGASQLM GENRTMTIHN GMFFSTYDRD NDGWLTSDPR KQCSKEDGGG WWYNRCHAAN PNGRYYWGGQ YTWDMAKHGT DDGVVWMNWK GSWYSMRKMS MKIRPFFPQQ

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 202-491 of human FGB (NP_005132.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,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 freeze / thaw cycles

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur Fibrinogen beta Chain

Antigène: Fibrinogen beta Chain (FGB)

Autre désignation: FGB (FGB Produits)

Sujet: The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including afibrinogenemia, dysfibrinogenemia, hypodysfibrinogenemia and thrombotic tendency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.,FGB,HEL-S-78p,Cardiovascular,Blood,Coagulation,FGB

Poids moléculaire: 55 kDa

ID gène: 2244

UniProt: P02675