Williams-Beuren Syndrome Chromosomal Region 16 Protein Homolog (WBS16) (AA 15-44), (N-Term) Antikörper Primary Antibody
WBS16
Reaktivität: Human, Hamster
WB
Wirt: Kaninchen
Polyclonal
unconjugated
camera_alt 1
Produktnummer ABIN5539310
$570.63
Zzgl. Versandkosten $45.00
400 μL
local_shipping
Lieferung nach:
Vereinigte Staaten von Amerika
Lieferung in 2 bis 3 Werktagen
-
- Target
- Williams-Beuren Syndrome Chromosomal Region 16 Protein Homolog (WBS16)
- Bindungsspezifität
-
AA 15-44, N-Term
- Reaktivität
- Human, Hamster
- Wirt
- Kaninchen
- Klonalität
- Polyklonal
- Konjugat
-
Unkonjugiert
- Applikation
-
Western Blotting (WB)
- Aufreinigung
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogen
- This WBS16 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 15-44 amino acids from the N-terminal region of human WBS16.
- Isotyp
- Ig Fraction
-
anti-Williams-Beuren Syndrome Chromosomal Region 16 Protein Homolog (WBS16) (AA 15-44), (N-Term) antibody Primary Antibody
WBS16 Reaktivität: Human, Hamster WB Wirt: Kaninchen Polyclonal RB27004 unconjugated
-
- Applikationshinweise
- For WB starting dilution is: 1:1000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Liquid
- Konzentration
- 0.5 mg/mL
- Buffer
- 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
- Informationen zur Lagerung
- Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
-
- Target
- Williams-Beuren Syndrome Chromosomal Region 16 Protein Homolog (WBS16)
- Andere Bezeichnung
- WBS16 ()
- 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. [provided by RefSeq].
- Molekulargewicht
- 50 kDa
- Gen-ID
- 81554
- UniProt
- Q96I51
Sie sind hier:
