GGNBP1 anticorps (AA 25-109) (AbBy Fluor® 350)

N° du produit ABIN1692737

L’anticorps Lapin Polyclonal anti-GGNBP1 a été validé pour WB, IF (cc) et IF (p). Il convient pour détecter GGNBP1 dans des échantillons de Humain.

Aperçu rapide pour GGNBP1 anticorps (AA 25-109) (AbBy Fluor® 350) (ABIN1692737)

Antigène: GGNBP1 (Gametogenetin Binding Protein 1 (GGNBP1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GGNBP1 est conjugé à/à la AbBy Fluor® 350

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

Détail du produit anti-GGNBP1 anticorps (AbBy Fluor® 350)

Épitope: AA 25-109

Homologie: Human

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human GGNBP1

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 GGNBP1

Antigène: GGNBP1 (Gametogenetin Binding Protein 1 (GGNBP1))

Autre désignation: GGNBP1

Sujet:

Synonyms: Gametogenetin-binding protein 1, GGNBP1, Putative gametogenetin-binding protein 1, GGNB1_HUMAN.

Background: GGNBP1 is a 109 amino acid protein that is thought to be involved in spermatogenesis and interacts with gametogenetin. GGNBP1 localizes to cytoplasm, membrane and Golgi apparatus, and exits as two isoforms which are produced by alternative splicing events. The gene encoding GGNBP1 maps to human chromosome 6, which contains 170 million base pairs and comprises nearly 6 % of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease, Stickler syndrome and a susceptibility to bipolar disorder are all associated with genes that map to chromosome 6.