C1orf114 Antikörper (AA 101-200) (Cy7)
-
- Target Alle C1orf114 (CCDC181) Antikörper anzeigen
- C1orf114 (CCDC181) (Coiled-Coil Domain Containing 181 (CCDC181))
-
Bindungsspezifität
- AA 101-200
-
Reaktivität
- Human, Maus
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser C1orf114 Antikörper ist konjugiert mit Cy7
-
Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human, Maus
- Homologie
- Rat,Cow,Sheep,Pig,Horse,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human C1orf114
- Isotyp
- IgG
- Top Product
- Discover our top product CCDC181 Primärantikörper
-
-
- Applikationshinweise
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
-
- Target
- C1orf114 (CCDC181) (Coiled-Coil Domain Containing 181 (CCDC181))
- Andere Bezeichnung
- C1orf114 (CCDC181 Produkte)
- Synonyme
- C1orf114 antikoerper, RP1-206D15.2 antikoerper, 4930455F23Rik antikoerper, AI427889 antikoerper, RGD1309708 antikoerper, coiled-coil domain containing 181 antikoerper, CCDC181 antikoerper, Ccdc181 antikoerper
- Hintergrund
-
Synonyms: C1orf114, CA114_HUMAN, chromosome 1 open reading frame 114, RP1-206D15.2, Uncharacterized protein C1orf114.
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. The C1orf114 gene product has been provisionally designated C1orf114 pending further characterization.
- Gen-ID
- 57821
-