GLYATL1 antibody (AA 101-200) (FITC)

Catalog No. ABIN1709214

Product Details anti-GLYATL1 Antibody (FITC)

Target: GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))

Binding Specificity: AA 101-200

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GLYATL1 antibody is conjugated to FITC

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

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GLYATL1

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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

Expiry Date: 12 months

Target Details for GLYATL1

Target: GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))

Alternative Name: GLYATL1 (GLYATL1 Products)

Synonyms: GATF-C antibody, GNAT antibody, glycine-N-acyltransferase like 1 antibody, GLYATL1 antibody

Background:

Synonyms: Acyl CoA glycine N acyltransferase like protein 1, EC 2.3.1.13, FLJ26507, FLJ34646, GATF C, GATFC, Glycine N acyltransferase like 1, GNAT, MGC15397, MGC15937, GLYL1_HUMAN.

Background: GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.