FAM59A anticorps (AA 151-250) (Alexa Fluor 594)

N° du produit ABIN2813091

Détail du produit anti-FAM59A anticorps (Alexa Fluor 594)

Antigène: FAM59A (Family with Sequence Similarity 59, Member A (FAM59A))

Épitope: AA 151-250

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM59A est conjugé à/à la Alexa Fluor 594

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM59A

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur FAM59A

Antigène: FAM59A (Family with Sequence Similarity 59, Member A (FAM59A))

Autre désignation: FAM59A (FAM59A Produits)

Synonymes: anticorps C18orf11, anticorps FAM59A, anticorps Gm944, anticorps C86169, anticorps Fam59a, anticorps mKIAA4238, anticorps fam59a, anticorps zgc:55634, anticorps GRB2 associated regulator of MAPK1 subtype 1, anticorps GRB2 associated, regulator of MAPK1, anticorps GAREM1, anticorps Garem1, anticorps garem

Sujet:

Synonyms: FA59A_HUMAN, fam59a, Family with sequence similarity 59, member A, GAREM, Gm944, Protein FAM59A.

Background: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterization.

ID gène: 64762

Pathways: EGFR Signaling Pathway