WBSCR16 Antikörper (N-Term)

Produktnummer ABIN2791205

Produktdetails anti-WBSCR16 Antikörper

Target: WBSCR16 (Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))

Bindungsspezifität: N-Term

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

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser WBSCR16 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: GYGFTLLSSK TADVTKVWGM GLNKDSQLGF HRSRKDKTRG YEYVLEPSPV

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

Produktmerkmale: This is a rabbit polyclonal antibody against WBSCR16. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human WBSCR16

Anwendungsinformationen

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

Kommentare:

Antigen size: 358 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 WBSCR16

Target: WBSCR16 (Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))

Andere Bezeichnung: WBSCR16 (WBSCR16 Produkte)

Synonyme: 5730496C04Rik antikoerper, AU019812 antikoerper, RCC1 like antikoerper, reculator of chromosome condensation 1 like antikoerper, RCC1L antikoerper, Rcc1l antikoerper

Hintergrund: This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Alias Symbols: WBSCR16
Protein Interaction Partner: UBC, NME6, ATXN1, BRCA1, SYNCRIP, HNRNPU, RBBP6, ICT1,
Protein Size: 358

Molekulargewicht: 40 kDa

Gen-ID: 81554

UniProt: Q8IW88