EFHA1 Antikörper (Alexa Fluor 594)

Produktnummer ABIN2812684

Produktdetails anti-EFHA1 Antikörper

Target: EFHA1 (EF-Hand Domain Family, Member A1 (EFHA1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser EFHA1 Antikörper ist konjugiert mit Alexa Fluor 594

Applikation: Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human EFHA1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 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.

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

Lagerung: -20 °C/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu EFHA1

Target: EFHA1 (EF-Hand Domain Family, Member A1 (EFHA1))

Andere Bezeichnung: EFHA1 (EFHA1 Produkte)

Synonyme: 1110008L20Rik antikoerper, EFHA1 antikoerper, Efha1 antikoerper, RGD1309934 antikoerper, Smhs2 antikoerper, 4833427E09Rik antikoerper, AU041871 antikoerper, mitochondrial calcium uptake 2 antikoerper, MICU2 antikoerper, Micu2 antikoerper

Hintergrund:

The EF-hand domain is a twelve amino acid loop motif that is commonly found in proteins that participate in calcium-binding events within the cell. EF-hand domains generally exist in a pair that, together, form a stable four-helix bundle that enables the binding of calcium ions. EF-HA1 (EF-hand domain family, member A1) is a 434 amino acid protein that contains four EF-hand domains, suggesting a role in calcium-mediated events throughout the cell. The gene encoding EF-HA1 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4 % of the human genome. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.

Synonyms: EF-HA1, EF hand domain containing family member A1, EF hand domain family A1, EF hand domain family member A1, EFHA1 EF hand domain family member A1, FLJ25016, FLJ34588, Smhs2 homolog, 1110008L20Rik, EFHA1_HUMAN.

Gen-ID: 221154