WBSCR22 Antikörper (C-Term)

Produktnummer ABIN2789228

Der Kaninchen Polyklonal Anti-WBSCR22-Antikörper wurde für WB validiert. Er ist geeignet, WBSCR22 in Proben von Human, Maus, Ratte, Hund, Rind (Kuh), Meerschweinchen, Pferd, Schwein und Kaninchen zu detektieren.

Kurzübersicht für WBSCR22 Antikörper (C-Term) (ABIN2789228)

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Reaktivität: Human, Maus, Ratte, Hund, Rind (Kuh), Meerschweinchen, Pferd, Schwein, Kaninchen

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser WBSCR22 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-WBSCR22 Antikörper

Bindungsspezifität: C-Term

Sequenz: GGAFERRGIR GHQTRRFPLR MSRRGMVRKS RAWVLEKKER HRRQGREVRP

Homologie: Cow: 77%, Dog: 86%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Mouse: 86%, Pig: 86%, Rabbit: 93%, Rat: 86%

Produktmerkmale: This is a rabbit polyclonal antibody against WBSCR22. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator.

Kommentare:

Antigen size: 298 AA

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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 freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Details zu WBSCR22

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Andere Bezeichnung: WBSCR22

Hintergrund: This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.
Alias Symbols: HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
Protein Interaction Partner: VCP, UBC, PKN1, OAS1, ZMYM3, THOC2, WDR74, REM1, PHLPP1, PPIP5K1, CUL3, SUMO2,
Protein Size: 298

Molekulargewicht: 32 kDa

Gen-ID: 114049

NCBI Accession: NM_001202560, NP_001189489

UniProt: C9K060