FAM55A Antikörper (AA 211-310) (Biotin)

Produktnummer ABIN6943432

Produktdetails anti-FAM55A Antikörper (Biotin)

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

Bindungsspezifität: AA 211-310

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM55A Antikörper ist konjugiert mit Biotin

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM55A

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Haltbarkeit: 12 months

Details zu FAM55A

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

Andere Bezeichnung: FAM55A (FAM55A Produkte)

Synonyme: FAM55A antikoerper, neurexophilin and PC-esterase domain family member 1 antikoerper, neurexophilin and PC-esterase domain family, member 1 antikoerper, NXPE1 antikoerper

Hintergrund:

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.

Gen-ID: 120400

UniProt: Q8N323