COL1A1 Antikörper (AA 1077-1106)

Produktnummer ABIN3030548

Der Kaninchen Polyklonal anti-COL1A1 Antikörper wird verwendet zum Nachweis von COL1A1 in Proben von Human und Maus. Er wurde validiert für WB, IHC und ELISA.

Kurzübersicht für COL1A1 Antikörper (AA 1077-1106) (ABIN3030548)

Target: COL1A1 (Collagen, Type I, alpha 1 (COL1A1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser COL1A1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Produktdetails anti-COL1A1 Antikörper

Bindungsspezifität: AA 1077-1106

Kreuzreaktivität (Details): Expected species reactivity: Rat, Bovine, Chicken

Aufreinigung: Antigen affinity purified

Immunogen: A portion of amino acids 1077-1106 from the human protein was used as the immunogen for this COL1A1 antibody.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Titration of the COL1A1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:10-1:50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Aliquot the COL1A1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Details zu COL1A1

Target: COL1A1 (Collagen, Type I, alpha 1 (COL1A1))

Andere Bezeichnung: COL1A1

Hintergrund: This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish].

UniProt: P02452

Pathways: Sensory Perception of Sound, Autophagie, Growth Factor Binding