Septin 9 anticorps

N° du produit ABIN7231314

Cet anticorps anti-Septin 9 est un anticorps Lapin Polyclonal détectant Septin 9 dans WB et ELISA. Adapté pour Humain.

Aperçu rapide pour Septin 9 anticorps (ABIN7231314)

Antigène: Septin 9 (SEPT9)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Septin 9 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Septin 9 anticorps

Fonction: SEPT9 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of SEPT9 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogène: Synthesized peptide derived from part region of human SEPT9 protein

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur Septin 9

Antigène: Septin 9 (SEPT9)

Autre désignation: SEPT9

Sujet: Rabbit Anti-SEPT9 Polyclonal Antibody,Septin-9, MLL septin-like fusion protein MSF-A, MLL septin-like fusion protein, Ovarian/Breast septin, Ov/Br septin, Septin D1,SEPT9 gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.,SEPT9

Poids moléculaire: observerd band 64kDa

ID gène: 10801

UniProt: Q9UHD8