CCBE1 Antikörper (AA 163-191)

Produktnummer ABIN5536650

Produktdetails anti-CCBE1 Antikörper

Target: CCBE1 (Collagen and Calcium Binding EGF Domains 1 (CCBE1))

Bindungsspezifität: AA 163-191

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CCBE1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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

Immunogen: This CCBE1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 163-191 amino acids from the Central region of human CCBE1.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Details zu CCBE1

Target: CCBE1 (Collagen and Calcium Binding EGF Domains 1 (CCBE1))

Andere Bezeichnung: CCBE1 (CCBE1 Produkte)

Synonyme: 4933426F18Rik antikoerper, 9430093N24Rik antikoerper, mKIAA1983 antikoerper, RGD1307670 antikoerper, fof antikoerper, collagen and calcium binding EGF domains 1 antikoerper, CCBE1 antikoerper, Ccbe1 antikoerper, ccbe1 antikoerper

Hintergrund: This gene is thought to function in extracellular matrix remodeling and migration. It is predominantly expressed in the ovary, but down regulated in ovarian cancer cell lines and primary carcinomas, suggesting its role as a tumour suppressor. Mutations in this gene have been associated with Hennekam lymphangiectasia-lymphedema syndrome, a generalized lymphatic dysplasia in humans.

Molekulargewicht: 44 kDa

Gen-ID: 147372

UniProt: Q6UXH8