FAM91A1 Antikörper (AA 335-440) (Alexa Fluor 680)

Produktnummer ABIN5002437

Produktdetails anti-FAM91A1 Antikörper (Alexa Fluor 680)

Target: FAM91A1 (Family with Sequence Similarity 91, Member A1 (FAM91A1))

Bindungsspezifität: AA 335-440

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM91A1 Antikörper ist konjugiert mit Alexa Fluor 680

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

Homologie: Human,Mouse,Rat,Chicken

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM91A1

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 FAM91A1

Target: FAM91A1 (Family with Sequence Similarity 91, Member A1 (FAM91A1))

Andere Bezeichnung: FAM91A1 (FAM91A1 Produkte)

Synonyme: AV220772 antikoerper, BC033609 antikoerper, Fam91a1 antikoerper, SKIN antikoerper, mKIAA0493 antikoerper, MGC63609 antikoerper, zgc:63609 antikoerper, family with sequence similarity 91, member A1 antikoerper, family with sequence similarity 91 member A1 antikoerper, Fam91a1 antikoerper, FAM91A1 antikoerper, fam91a1 antikoerper

Hintergrund:

Synonyms: FAM91A1, Family with sequence similarity 91 member A1, FLJ23790, Hypothetical protein LOC157769, LOC157769, F91A1_HUMAN.

Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM91A1 gene product has been provisionally designated FAM91A1 pending further characterization.

Gen-ID: 157769