FAM82A1 Antikörper (AA 261-360) (Biotin)

Produktnummer ABIN1398355

Produktdetails anti-FAM82A1 Antikörper (Biotin)

Target: FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))

Bindungsspezifität: AA 261-360

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAM82A1 Antikörper ist konjugiert mit Biotin

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

Homologie: Human,Mouse,Rat,Dog,Pig,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM82A1

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 FAM82A1

Target: FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))

Andere Bezeichnung: FAM82A1 (RMDN2 Produkte)

Synonyme: FAM82A antikoerper, FAM82A1 antikoerper, PRO34163 antikoerper, PYST9371 antikoerper, RMD-2 antikoerper, RMD2 antikoerper, RMD4 antikoerper, regulator of microtubule dynamics 2 antikoerper, RMDN2 antikoerper

Hintergrund:

Synonyms: BLOCK18, FAM82A, Fam82a1, Family with sequence similarity 82 member A, Family with sequence similarity 82, member A1, hRMD 2, hRMD 4, hRMD-2, hRMD4, MGC33318, Microtubule associated protein, Protein FAM82A1, Regulator of microtubule dynamics, Regulator of microtubule dynamics protein 2, RMD 2, RMD-2, RMD2, RMD2_HUMAN.

Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FAM82A gene product has been provisionally designated FAM82A pending further characterization.