ZBTB40 anticorps (AA 851-950) (Biotin)

N° du produit ABIN1700573

Détail du produit anti-ZBTB40 anticorps (Biotin)

Antigène: ZBTB40 (Zinc Finger and BTB Domain Containing 40 (ZBTB40))

Épitope: AA 851-950

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ZBTB40 est conjugé à/à la Biotin

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human ZBTB40

Isotype: IgG

Information d'application

Indications d'application: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur ZBTB40

Antigène: ZBTB40 (Zinc Finger and BTB Domain Containing 40 (ZBTB40))

Autre désignation: ZBTB40 (ZBTB40 Produits)

Synonymes: anticorps ZNF923, anticorps BC059177, anticorps C230087D24, anticorps Gm571, anticorps mKIAA0478, anticorps RGD1309866, anticorps zinc finger and BTB domain containing 40, anticorps ZBTB40, anticorps Zbtb40

Sujet:

Synonyms: BC059177, C230087D24, Gm571, KIAA0478, MGC133098, MGC62412, mKIAA0478, RGD1309866, RP23 95O23.1, ZBT40_HUMAN, ZBTB40, Zinc finger and BTB domain containing 40, Zinc finger and BTB domain containing protein 40, Zinc finger and BTB domain-containing protein 40, ZNF923.

Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

ID gène: 9923