CST3 anticorps

N° du produit ABIN7148973

Détail du produit anti-CST3 anticorps

Antigène: CST3 (Cystatin C (CST3))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp CST3 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Réactivité croisée: Humain

Purification: Protein G purified

Immunogène: Recombinant Human Cystatin C protein

Clone: 3A1B7

Isotype: IgG2b

Information d'application

Indications d'application: Recommended dilution:IHC:1:50-1:500,

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Preservative: 0.03 % Proclin 300
Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C,-80 °C

Stockage commentaire: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Détails sur CST3

Antigène: CST3 (Cystatin C (CST3))

Autre désignation: CST3 (CST3 Produits)

Synonymes: anticorps armd11, anticorps fb51d07, anticorps wu:fb24g06, anticorps wu:fb51d07, anticorps wu:fc55f03, anticorps zgc:136227, anticorps ARMD11, anticorps CysC, anticorps CYSC, anticorps cystatin C, anticorps cystatin C L homeolog, anticorps cystatin C (amyloid angiopathy and cerebral hemorrhage), anticorps cystatin 3, anticorps CST3, anticorps cst3.L, anticorps cst3, anticorps cystatin 3, anticorps Cst3

Sujet:

Background: Defects in CST3 are the cause of amyloidosis type 6 (AMYL6) [MIM:105150], also known as hereditary cerebral hemorrhage with amyloidosis (HCHWA), cerebral amyloid angiopathy (CAA) or cerebroarterial amyloidosis Icelandic type. AMYL6 is a hereditary generalized amyloidosis due to cystatin C amyloid deposition. Cystatin C amyloid accumulates in the walls of arteries, arterioles, and sometimes capillaries and veins of the brain, and in various organs including lymphoid tissue, spleen, salivary glands, and seminal vesicles. Amyloid deposition in the cerebral vessels results in cerebral amyloid angiopathy, cerebral hemorrhage and premature stroke. Cystatin C levels in the cerebrospinal fluid are abnormally low.Genetic variations in CST3 are associated with age-related macular degeneration type 11 (ARMD11) [MIM:611953]. ARMD is a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.

Aliases: CysC,Cystatin-3,Gamma-trace,Neuroendocrine basic polypeptide,Post-gamma-globulin

UniProt: P01034