TRIM37 Antikörper (C-Term)

Produktnummer ABIN657211

Produktdetails anti-TRIM37 Antikörper

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

Bindungsspezifität: AA 936-964, C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TRIM37 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This TRIM37 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 936-964 amino acids from the C-terminal region of human TRIM37.

Klon: RB33250

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Haltbarkeit: 6 months

Details zu TRIM37

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

Andere Bezeichnung: TRIM37 (TRIM37 Produkte)

Synonyme: MUL antikoerper, POB1 antikoerper, TEF3 antikoerper, 1110032A10Rik antikoerper, 2810004E07Rik antikoerper, AI848587 antikoerper, AU043018 antikoerper, mKIAA0898 antikoerper, tripartite motif-containing 37 antikoerper, tripartite motif containing 37 antikoerper, Trim37 antikoerper, TRIM37 antikoerper

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: 107906

NCBI Accession: NP_001005207, NP_056109

UniProt: O94972