Dynein Regulatory Complex Subunit 1 (DRC1) (AA 301-400) Antikörper (Alexa Fluor 594)

Produktnummer ABIN2810794

Produktdetails

Target: Dynein Regulatory Complex Subunit 1 (DRC1)

Bindungsspezifität: AA 301-400

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Alexa Fluor 594

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

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C2orf39

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

Antigendetails

Target: Dynein Regulatory Complex Subunit 1 (DRC1)

Andere Bezeichnung: C2orf39 (DRC1 Produkte)

Synonyme: C2orf39 antikoerper, CCDC164 antikoerper, CILD21 antikoerper, Ccdc164 antikoerper, Gm1060 antikoerper, b2b1654Clo antikoerper, C11H2orf39 antikoerper, c2orf39 antikoerper, ccdc164 antikoerper, QtsA-11540 antikoerper, QtsA-14589 antikoerper, QtsA-15139 antikoerper, QtsA-15601 antikoerper, QtsA-16686 antikoerper, sb:eu1661 antikoerper, si:dkey-65b13.6 antikoerper, C3H2orf39 antikoerper, dynein regulatory complex subunit 1 antikoerper, dynein regulatory complex subunit 1 L homeolog antikoerper, dynein regulatory complex subunit 1 homolog (Chlamydomonas) antikoerper, DRC1 antikoerper, Drc1 antikoerper, drc1.L antikoerper, drc1 antikoerper

Hintergrund:

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 C2orf39 gene product has been provisionally designated C2orf39 pending further characterization.

Subcellular location: Cytoplasm

Synonyms: CC164_HUMAN, CCDC164, Coiled-coil domain-containing protein 164.

Gen-ID: 92749