Factor XI anticorps (AA 1-282)

N° du produit ABIN1885884

Cet anticorps anti-Factor XI Polyclonal Lapin (ABIN1885884) détecte spécifiquement Factor XI dans WB et IHC. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Factor XI anticorps (AA 1-282) (ABIN1885884)

Antigène: Factor XI (F11) (Coagulation Factor XI (F11))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Factor XI est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-Factor XI anticorps

Épitope: AA 1-282

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 282 of Human F11

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.250

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur Factor XI

Antigène: Factor XI (F11) (Coagulation Factor XI (F11))

Autre désignation: Factor XI

Sujet: This gene encodes coagulation factor XI of the blood coagulation cascade.This protein is present in plasma as a zymogen, which is a unique plasma coagulation enzyme because it exists as a homodimer consisting of two identical polypeptide chains linked by disulfide bonds.During activation of the plasma factor XI, an internal peptide bond is cleaved by factor XIIa (or XII) in each of the two chains, resulting in activated factor XIa, a serine protease composed of two heavy and two light chains held together by disulfide bonds.This activated plasma factor XI triggers the middle phase of the intrisic pathway of blood coagulation by activating factor IX.Defects in this factor lead to Rosenthal syndrome, a blood coagulation abnormality.[provided by RefSeq]

Poids moléculaire: 70 kDa

ID gène: 2160

NCBI Accession: NP_000119, NM_000128