GLB1L3 anticorps (AA 51-150)

N° du produit ABIN1388013

Cet anticorps anti-GLB1L3 est un anticorps Lapin Polyclonal détectant GLB1L3 dans WB, ELISA, IF (cc), IF (p), IHC (p) et IHC (fro). Adapté pour Souris.

Aperçu rapide pour GLB1L3 anticorps (AA 51-150) (ABIN1388013)

Antigène: GLB1L3 (Galactosidase, beta 1-Like 3 (GLB1L3))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GLB1L3 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-GLB1L3 anticorps

Épitope: AA 51-150

Réactivité croisée: Souris

Homologie: Human,Rat,Horse,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human GLB1L3

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur GLB1L3

Antigène: GLB1L3 (Galactosidase, beta 1-Like 3 (GLB1L3))

Autre désignation: GLB1L3

Sujet:

Synonyms: Beta galactosidase 1 like protein 3, Beta-galactosidase-1-like protein 3, FLJ90231, Galactosidase, beta 1 like 3, GLB1L 3, Glb1l3, GLBL3_HUMAN, LOC112937, OTTHUMP00000235427.

Background: GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.