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

Produktnummer ABIN896702

Produktdetails anti-FAM89B Antikörper (Alexa Fluor 350)

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

Bindungsspezifität: AA 41-150

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM89B Antikörper ist konjugiert mit Alexa Fluor 350

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

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

Aufreinigung: Purified by Protein A.

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

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

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu FAM89B

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

Andere Bezeichnung: FAM89B (FAM89B Produkte)

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

Hintergrund:

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.

Gen-ID: 23625