GTDC1 antibody (Glycosyltransferase-Like Domain Containing 1) AA 361-458 (Alexa Fluor 555)

Catalog No. ABIN1399859

Product Details anti-GTDC1 Antibody

Target: GTDC1

Binding Specificity: AA 361-458

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GTDC1 antibody is conjugated to Alexa Fluor 555

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

Predicted Reactivity: Human,Mouse,Rat,Dog,Pig,Horse,Rabbit,Zebrafish

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GTDC1

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.

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

Storage: -20 °C/-80 °C

Storage Comment: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Expiry Date: 12 months

Target Details for GTDC1

Target: GTDC1

Alternative Name: GTDC1 (GTDC1 Products)

Synonyms: Hmat-Xa, mat-Xa, E330008O22Rik, zgc:110568, glycosyltransferase like domain containing 1, glycosyltransferase-like domain containing 1, glycosyltransferase like domain containing 1 S homeolog, GTDC1, Gtdc1, gtdc1.S, gtdc1

Background:

Glycosyltransferases that mediate the regio- and stereoselective transfer of sugars, such as the fucosyltransferases, determine cell surface-carbohydrate profiles, which is an essential interface for biological recognition processes. GTDC1 (Glycosyltransferase-like domain-containing protein 1), also known as Mat-Xa, is a 458 amino acid protein belonging to the glycosyltransferase 1 family. GTDC1 is ubiquitously expressed, with highest levels found in peripheral blood leukocytes, spleen, lung and testis.An extremely rare recessive genetic disorder, Alstr syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.

Synonyms: Glycosyltransferase like 1, Glycosyltransferase like domain containing 1, Glycosyltransferase like domain containing protein 1, Mannosyltransferase candidate, GTDC1_HUMAN.

Gene ID: