TRIM37 Antikörper (AA 902-964)

Produktnummer ABIN1886711

Der Kaninchen Polyklonal Anti-TRIM37-Antikörper wurde für WB, IHC und IF validiert. Er ist geeignet, TRIM37 in Proben von Human zu detektieren.

Kurzübersicht für TRIM37 Antikörper (AA 902-964) (ABIN1886711)

Target: TRIM37 (Tripartite Motif Containing 37 (TRIM37))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TRIM37 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Produktdetails anti-TRIM37 Antikörper

Bindungsspezifität: AA 902-964

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Synthetic peptide contain a sequence corresponding to a region within amino acids 902 and 964 of TRIM37

Anwendungsinformationen

Applikationshinweise: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.1000
Immunofluorescence: 1.100-1.200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: Biohazard Informations: This product contains thimerosal which is hazardous.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Details zu TRIM37

Target: TRIM37 (Tripartite Motif Containing 37 (TRIM37))

Andere Bezeichnung: TRIM37

Hintergrund: This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis.The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain.The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions.The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin.Alternatively spliced transcript variants encoding the same protein have been identified.[provided by RefSeq]

Molekulargewicht: 108 kDa

Gen-ID: 4591

NCBI Accession: NM_001005207, NP_001005207