VAT1L anticorps (AA 321-419) (Biotin)

N° du produit ABIN1389451

Détail du produit anti-VAT1L anticorps (Biotin)

Antigène: VAT1L (Vesicle Amine Transport 1-Like (VAT1L))

Épitope: AA 321-419

Reactivité: Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp VAT1L est conjugé à/à la Biotin

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

Réactivité croisée: Rat

Homologie: Human,Mouse,Dog,Cow,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human VAT1L/KIAA1576

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
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 VAT1L

Antigène: VAT1L (Vesicle Amine Transport 1-Like (VAT1L))

Autre désignation: VAT1L/KIAA1576 (VAT1L Produits)

Synonymes: anticorps VAT1L, anticorps 9430073I07, anticorps AI427515, anticorps mKIAA1576, anticorps zgc:171879, anticorps vesicle amine transport 1 like, anticorps vesicle amine transport protein 1 like, anticorps vesicle amine transport 1-like, anticorps VAT1L, anticorps Vat1l, anticorps vat1l

Sujet:

Synonyms: Probable oxidoreductase KIAA1576, Synaptic vesicle membrane protein VAT 1 homolog like, Synaptic vesicle membrane protein VAT-1 homolog-like, VAT 1L, VAT1L, VAT1L_HUMAN, Vesicle amine transport protein 1 homolog T. calornica like.

Background: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier. The KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.

ID gène: 3384