TMEM184B Antikörper (C-Term)

Produktnummer ABIN500976

Produktdetails anti-TMEM184B Antikörper

Target: TMEM184B (Transmembrane Protein 184B (TMEM184B))

Bindungsspezifität: C-Term

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TMEM184B Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Spezifität: This antibody detects TMEM184B near C-term.

Aufreinigung: Peptide affinity chromatography

Immunogen: TMEM184B antibody was raised against a 15 amino acid peptide near the carboxy terminus of human TMEM184B.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: ELISA. Western blot.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1.0 mg/mL

Buffer: PBS containing 0.02 % sodium azide

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu TMEM184B

Target: TMEM184B (Transmembrane Protein 184B (TMEM184B))

Andere Bezeichnung: TMEM184B (TMEM184B Produkte)

Synonyme: C22orf5 antikoerper, FM08 antikoerper, HS5O6A antikoerper, 2610507A11 antikoerper, 4732495E13Rik antikoerper, RGD1306591 antikoerper, TMEM148B antikoerper, transmembrane protein 184ba antikoerper, transmembrane protein 184B antikoerper, transmembrane protein 184b antikoerper, tmem184ba antikoerper, Tsp_04618 antikoerper, TMEM184B antikoerper, Tmem184b antikoerper

Hintergrund: TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22, mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.Synonyms: C22orf5, Putative MAPK-activating protein FM08, Transmembrane protein 184B

Gen-ID: 25829

NCBI Accession: NP_036396