FAM55A anticorps (AA 211-310) (Alexa Fluor 647)

N° du produit ABIN6979955

Détail du produit anti-FAM55A anticorps (Alexa Fluor 647)

Antigène: FAM55A (Family with Sequence Similarity 55, Member A (FAM55A))

Épitope: AA 211-310

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM55A est conjugé à/à la Alexa Fluor 647

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

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM55A

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 FAM55A

Antigène: FAM55A (Family with Sequence Similarity 55, Member A (FAM55A))

Autre désignation: FAM55A (FAM55A Produits)

Synonymes: anticorps FAM55A, anticorps neurexophilin and PC-esterase domain family member 1, anticorps neurexophilin and PC-esterase domain family, member 1, anticorps NXPE1

Sujet:

Synonyms: FA55A_HUMAN, FAM55A, Family with sequence similarity 55, member A, Hypothetical protein LOC120400, MGC34290, Neurexophilin and PC-esterase domain family, member 1, NXPE family member 1, NXPE1, OTTHUMP00000238511, Protein FAM55A.

Background: With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM55A gene product has been provisionally designated FAM55A pending further characterization.

ID gène: 120400

UniProt: Q8N323