GTDC1 antibody (Glycosyltransferase-Like Domain Containing 1) AA 361-458 (Alexa Fluor 555) Primary Antibody
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- Target See all GTDC1 Antibodies
- GTDC1
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Binding Specificity
- AA 361-458
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This GTDC1 antibody is conjugated to Alexa Fluor 555
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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
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- Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- 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
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- 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
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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