NSG2 anticorps (AA 31-140) (Alexa Fluor 350)

N° du produit ABIN1394787

Détail du produit anti-NSG2 anticorps (Alexa Fluor 350)

Antigène: NSG2 (HMP19) (Neuron-Specific Protein Family Member 2 (HMP19))

Épitope: AA 31-140

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NSG2 est conjugé à/à la Alexa Fluor 350

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Mouse,Rat,Cow,Pig,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human NSG2/HMP19

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur NSG2

Antigène: NSG2 (HMP19) (Neuron-Specific Protein Family Member 2 (HMP19))

Autre désignation: NSG2 (HMP19 Produits)

Synonymes: anticorps NSG2, anticorps 8.5, anticorps AA989750, anticorps R75287, anticorps neuronal vesicle trafficking associated 2, anticorps neuron specific gene family member 2, anticorps NSG2, anticorps Nsg2

Sujet:

Synonyms: HMP19, Neuron-specic protein family member 2, Nsg2, NSG2_HUMAN, Protein p19.

Background: With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.