NDUFAF7 Antikörper (AA 101-200) (Alexa Fluor 594)

Produktnummer ABIN2810802

Produktdetails anti-NDUFAF7 Antikörper

Target: NDUFAF7 (NADH Dehydrogenase (Ubiquinone) Complex I, Assembly Factor 7 (NDUFAF7))

Bindungsspezifität: AA 101-200

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NDUFAF7 Antikörper ist konjugiert mit Alexa Fluor 594

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

Homologie: Human,Mouse,Rat,Cow,Sheep,Pig,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C2orf56

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.

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 NDUFAF7

Target: NDUFAF7 (NADH Dehydrogenase (Ubiquinone) Complex I, Assembly Factor 7 (NDUFAF7))

Andere Bezeichnung: C2orf56 (NDUFAF7 Produkte)

Synonyme: C11H2orf56 antikoerper, 2410091C18Rik antikoerper, AL033374 antikoerper, PRO1853 antikoerper, C2orf56 antikoerper, MidA antikoerper, c2orf56 antikoerper, NADH:ubiquinone oxidoreductase complex assembly factor 7 antikoerper, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 7 antikoerper, NADH:ubiquinone oxidoreductase complex assembly factor 7 S homeolog antikoerper, NDUFAF7 antikoerper, Ndufaf7 antikoerper, ndufaf7.S antikoerper

Hintergrund:

C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare 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 related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

Subcellular location: Cytoplasm

Synonyms: C2orf56, Chromosome 2 open reading frame 56, MidA, MIDA_HUMAN, mitochondrial, Mitochondrial dysfunction protein A homolog, OTTHUMP00000158583, OTTHUMP00000201359, OTTHUMP00000201362, PRO1853, Protein midA homolog, Protein midA homolog, mitochondrial.

Gen-ID: 55471