FAM89B anticorps (AA 41-150) (Alexa Fluor 350)

N° du produit ABIN896702

Détail du produit anti-FAM89B anticorps (Alexa Fluor 350)

Antigène: FAM89B (Family with Sequence Similarity 89, Member B (FAM89B))

Épitope: AA 41-150

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM89B est conjugé à/à la Alexa Fluor 350

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

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM89B/MMTV-R

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 FAM89B

Antigène: FAM89B (Family with Sequence Similarity 89, Member B (FAM89B))

Autre désignation: FAM89B (FAM89B Produits)

Synonymes: anticorps MTVR1, anticorps 1110021A21Rik, anticorps MMTV, anticorps Mtvr2, anticorps family with sequence similarity 89 member B, anticorps family with sequence similarity 89, member B, anticorps FAM89B, anticorps Fam89b

Sujet:

Synonyms: Family with sequence similarity 89 member B, Mammary tumor virus receptor 2v Mammary turmor virus receptor homolog 1, MMTVR, MMTVR2, MTVR1, Protein FAM89B, FA89B_HUMAN.

Background: Mtvr1 is a 176 amino acid protein that exists as two alternatively spliced isoforms. Belonging to the FAM89 family, Mtvr1 is encoded by a gene that maps to human chromosome 11, which comprises approximately 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, while 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-encoded genes.

ID gène: 23625