BCL7B Antikörper (C-Term)

Produktnummer ABIN1536707

Der Kaninchen Polyklonal Anti-BCL7B-Antikörper wurde für WB und IHC (p) validiert. Er ist geeignet, BCL7B in Proben von Human und Maus zu detektieren.

Kurzübersicht für BCL7B Antikörper (C-Term) (ABIN1536707)

Target: BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BCL7B Antikörper ist unkonjugiert

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

Klon: RB36546

Produktdetails anti-BCL7B Antikörper

Bindungsspezifität: AA 137-164, C-Term

Homologie: B

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

Immunogen: This BCL7B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 137-164 amino acids from the C-terminal region of human BCL7B.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000. 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: BCL7B Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu BCL7B

Target: BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))

Andere Bezeichnung: BCL7B

Hintergrund: This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene.

Molekulargewicht: 22195

Gen-ID: 9275

NCBI Accession: NP_001184173, NP_001698

UniProt: Q9BQE9