MITF Antikörper (N-Term)

Produktnummer ABIN6295495

Dieses Maus Monoklonal-Antikörper erkennt spezifisch MITF in IHC, IF und FACS. Er zeigt eine Reaktivität gegenüber Human.

Kurzübersicht für MITF Antikörper (N-Term) (ABIN6295495)

Target: MITF (Microphthalmia-Associated Transcription Factor (MITF))

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser MITF Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)

Produktdetails anti-MITF Antikörper

Bindungsspezifität: N-Term

Verwendungszweck: Mouse anti-Human MITF Antibody Cocktail [Sodium Azide Free]

Spezifität: Nuclear

Aufreinigung: An N-terminus fragment (D5) and recombinant human protein (MITF/915) were used as the immunogen for the MITF antibody cocktail.

Immunogen: An N-terminus fragment (D5) and recombinant human protein (MITF/915) were used as the immunogen for the MITF antibody cocktail.

Anwendungsinformationen

Applikationshinweise: Flow Cytometry: 0.5-1 μg/million cells in 0.1ml
Immunofluorescence: 0.5-1 μg/mL
Immunohistochemistry (FFPE): 0.5-1 μg/mL for 30 min at RT (1)
Prediluted format: incubate for 30 min at RT (2)

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: In 1X PBS, BSA free, sodium azide free

Konservierungsmittel: Azide free

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 2-8°C. The azide-free format should be aliquoted and stored at -20°C or colder.

Details zu MITF

Target: MITF (Microphthalmia-Associated Transcription Factor (MITF))

Andere Bezeichnung: Microphthalmia-associated transcription factor

Hintergrund:

Target Description: MITF (microphthalmia transcription factor) is a basic helix-loop-helix-leucine-zipper (bHLH-Zip) transcription factor that regulates the development and survival of melanocytes and retinal pigment epithelium, and also is involved in transcription of pigmentation enzyme genes such as tyrosinase TRP1 and TRP2. MITF has been shown to be phosphorylated by MAP kinase in response to c-kit activation, resulting in upregulation of MITF transcriptional activity. Mutations of the MITF gene are associated with the autosomal dominant hereditary deafness and pigmentation condition, Waardenburg Syndrome type 2A. Multiple isoforms of MITF exist, including MITF-A, MITF-B, MITF-C, MITF-H, and MITF-M, which differ in the amino-terminal domain and in their expression patterns. The MITF-M isoform is restricted to the melanocyte cell lineage. Anti-MITF, D5, recognizes a nuclear protein, which is expressed in the majority of primary and metastatic epithelioid malignant melanomas as well as in normal melanocytes, benign nevi and dysplastic nevi.

Gene Symbol: MITF///BHLHE32

Gen-ID: 4286

UniProt: O75030

Pathways: Chromatin Binding