FBLN4 anticorps (AA 26-250)

N° du produit ABIN6139957

Cet anticorps Lapin Polyclonal détecte spécifiquement FBLN4 dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour FBLN4 anticorps (AA 26-250) (ABIN6139957)

Antigène: FBLN4 (Fibulin 4 (FBLN4))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FBLN4 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-FBLN4 anticorps

Épitope: AA 26-250

Séquence: SPQDSEEPDS YTECTDGYEW DPDSQHCRDV NECLTIPEAC KGEMKCINHY GGYLCLPRSA AVINDLHGEG PPPPVPPAQH PNPCPPGYEP DDQDSCVDVD ECAQALHDCR PSQDCHNLPG SYQCTCPDGY RKIGPECVDI DECRYRYCQH RCVNLPGSFR CQCEPGFQLG PNNRSCVDVN ECDMGAPCEQ RCFNSYGTFL CRCHQGYELH RDGFSCSDID ECSYS

Réactivité croisée: Humain

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 26-250 of human EFEMP2 (NP_058634.4).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:1000

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.

Stock: -20 °C

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

Détails sur FBLN4

Antigène: FBLN4 (Fibulin 4 (FBLN4))

Autre désignation: EFEMP2

Sujet: A large number of extracellular matrix proteins have been found to contain variations of the epidermal growth factor (EGF) domain and have been implicated in functions as diverse as blood coagulation, activation of complement and determination of cell fate during development. The protein encoded by this gene contains four EGF2 domains and six calcium-binding EGF2 domains. This gene is necessary for elastic fiber formation and connective tissue development. Defects in this gene are cause of an autosomal recessive cutis laxa syndrome. Alternatively spliced transcript variants have been identified for this gene.,EFEMP2,ARCL1B,FBLN4,MBP1,UPH1,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,EFEMP2

Poids moléculaire: 49 kDa

ID gène: 30008

UniProt: O95967