GLYCTK antibody (AA 251-350) (AbBy Fluor® 594)

Catalog No. ABIN2814157

The Rabbit Polyclonal anti-GLYCTK antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect GLYCTK in samples from Mouse.

Quick Overview for GLYCTK antibody (AA 251-350) (AbBy Fluor® 594) (ABIN2814157)

Target: GLYCTK (Glycerate Kinase (GLYCTK))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GLYCTK antibody is conjugated to AbBy Fluor® 594

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

Product Details anti-GLYCTK Antibody (AbBy Fluor® 594)

Binding Specificity: AA 251-350

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HBEBP2/GLYCTK

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 GLYCTK

Target: GLYCTK (Glycerate Kinase (GLYCTK))

Alternative Name: HBEBP2/GLYCTK

Background:

Synonyms: CG9886 like, GLCTK_HUMAN, Glycerate kinase, Glyctk, GLYCTK1, HBeAg binding protein 2, HBeAg binding protein 4, HBeAg-binding protein 4, HBeAgBP4A, HBEBP2, HBEBP4.

Background: GLYCTK is a 523 amino acid protein that is expressed as seven isoforms which are present throughout the body. Localized to the cytoplasm and the mitochondrion in an isoform-specific manner, GLYCTK functions to catalyze the ATP-dependent conversion of (R)-glycerate to 3-(R)-glycerate, thereby playing an important role in neural and skeletal muscle systems. Defects in the gene encoding GLYCTK are the cause of D-glyceric acidemia, an inborn error of amino acid metabolism that is best described as nonketotic hyperglycinemia and is characterized by the excretion of D-glyceric acid in the urine.

Gene ID: 132158