GLB1L3 antibody (AA 51-150) (Biotin)

Catalog No. ABIN1398919

Product Details anti-GLB1L3 Antibody (Biotin)

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

Binding Specificity: AA 51-150

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GLB1L3 antibody is conjugated to Biotin

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

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Horse,Chicken

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GLB1L3

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for GLB1L3

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

Alternative Name: GLB1L3 (GLB1L3 Products)

Synonyms: 4921509F24Rik antibody, GLB1L3 antibody, galactosidase, beta 1 like 3 antibody, galactosidase beta 1 like 2 antibody, galactosidase beta 1 like 3 antibody, galactosidase, beta 1-like 3 antibody, Glb1l3 antibody, GLB1L2 antibody, GLB1L3 antibody

Background:

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.