INF2 anticorps (AA 589-616)

N° du produit ABIN5539055

Détail du produit anti-INF2 anticorps

Antigène: INF2 (Inverted Formin, FH2 and WH2 Domain Containing (INF2))

Épitope: AA 589-616

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp INF2 est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This INF2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 589-616 amino acids from the Central region of human INF2.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur INF2

Antigène: INF2 (Inverted Formin, FH2 and WH2 Domain Containing (INF2))

Autre désignation: INF2 (INF2 Produits)

Synonymes: anticorps C14orf151, anticorps C14orf173, anticorps CMTDIE, anticorps FSGS5, anticorps pp9484, anticorps 2610204M08Rik, anticorps AA589465, anticorps AW125550, anticorps EG629699, anticorps inverted formin, FH2 and WH2 domain containing, anticorps INF2, anticorps Inf2

Sujet: This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5.

Poids moléculaire: 136 kDa

ID gène: 64423

UniProt: Q27J81