TBL2 Antikörper (N-Term)

Produktnummer ABIN656760

Produktdetails anti-TBL2 Antikörper

Target: TBL2 (Transducin (Beta)-Like 2 (TBL2))

Bindungsspezifität: AA 43-72, N-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TBL2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This TBL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 43-72 amino acids from the N-terminal region of human TBL2.

Klon: RB32541

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000. IHC-P: 1:10~50

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody 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: TBL2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Haltbarkeit: 6 months

Details zu TBL2

Target: TBL2 (Transducin (Beta)-Like 2 (TBL2))

Andere Bezeichnung: TBL2 (TBL2 Produkte)

Synonyme: wu:fa96f08 antikoerper, tbl2 antikoerper, MGC53692 antikoerper, TBL2 antikoerper, MGC79804 antikoerper, MGC140759 antikoerper, DKFZp469O1728 antikoerper, WBSCR13 antikoerper, WS-betaTRP antikoerper, C76179 antikoerper, WS-bTRP antikoerper, transducin (beta)-like 2 antikoerper, transducin (beta)-like 2 L homeolog antikoerper, transducin beta like 2 antikoerper, tbl2 antikoerper, tbl2.L antikoerper, TBL2 antikoerper, Tbl2 antikoerper

Hintergrund: This gene encodes a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.

Molekulargewicht: 49798

Gen-ID: 26608

NCBI Accession: NP_036585

UniProt: Q9Y4P3