ZBTB40 Antikörper (AA 851-950) (Biotin)

Produktnummer ABIN1700573

Produktdetails anti-ZBTB40 Antikörper (Biotin)

Target: ZBTB40 (Zinc Finger and BTB Domain Containing 40 (ZBTB40))

Bindungsspezifität: AA 851-950

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ZBTB40 Antikörper ist konjugiert mit Biotin

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

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human ZBTB40

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: 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 ZBTB40

Target: ZBTB40 (Zinc Finger and BTB Domain Containing 40 (ZBTB40))

Andere Bezeichnung: ZBTB40 (ZBTB40 Produkte)

Synonyme: ZNF923 antikoerper, BC059177 antikoerper, C230087D24 antikoerper, Gm571 antikoerper, mKIAA0478 antikoerper, RGD1309866 antikoerper, zinc finger and BTB domain containing 40 antikoerper, ZBTB40 antikoerper, Zbtb40 antikoerper

Hintergrund:

Synonyms: BC059177, C230087D24, Gm571, KIAA0478, MGC133098, MGC62412, mKIAA0478, RGD1309866, RP23 95O23.1, ZBT40_HUMAN, ZBTB40, Zinc finger and BTB domain containing 40, Zinc finger and BTB domain containing protein 40, Zinc finger and BTB domain-containing protein 40, ZNF923.

Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

Gen-ID: 9923