Recombinant Human ALG3 Protein

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, ELISA, PA

Order Details

Recombinant Human ALG3 Protein Summary

Description
A recombinant protein with GST tag at N-terminal corresponding to the amino acids 1-438 of Human ALG3 full-length ORF

Source: Wheat Germ (in vitro)

Amino Acid Sequence:MAAGLRKRGRSGSAAQAEGLCKQWLQRAWQERRLLLREPRYTLLVAACLCLAEVGITFWVIHRVAYTEIDWKAYMAEVEGVINGTYDYTQLQGDTGPLVYPAGFVYIFMGLYYATSRGTDIRMAQNIFAVLYLATLLLVFLIYHQTCKVPPFVFFFMCCASYRVHSIFVLRLFNDPVAMVLLFLSINLLLAQRWGWGCCFFSLAVSVKMNVLLFAPGLLFLLLTQFGFRGALPKLGICAGLQVVLGLPFLLENPSGYLSRSFDLGRQFLFHWTVNWRFLPEALFLHRAFHLALLTAHLTLLLLFALCRWHRTGESILSLLRDPSKRKVPPQPLTPNQIVSTLFTSNFIGICFSRSLHYQFYVWYFHTLPYLLWAMPARWLTHLLRLLVLGLIELSWNTYPSTSCSSAALHICHAVILLQLWLGPQPFPKSTQHSKKAH

Protein/Peptide Type
Recombinant Protein
Gene
ALG3

Applications/Dilutions

Application Notes
This protein has not been tested for any functionality. Product may contain endotoxins and is not suitable for use with live cells.

Packaging, Storage & Formulations

Storage
Store at -80C. Avoid freeze-thaw cycles.
Buffer
50 mM Tris-HCl, 10 mM reduced Glutathione, pH 8.0 in the elution buffer.

Notes

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for Recombinant Human ALG3 Protein

  • alpha-1,3-mannosyltransferase)
  • asparagine-linked glycosylation 3 homolog (S. cerevisiae
  • asparagine-linked glycosylation 3 homolog (yeast
  • asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog (S.cerevisiae)
  • Asparagine-linked glycosylation protein 3 homolog
  • carbohydrate deficient glycoprotein syndrome type IV
  • CDGS4D16Ertd36e
  • Dolichyl-phosphate-mannose--glycolipid alpha-mannosyltransferase
  • dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase
  • dol-P-Man dependent alpha(1-3)-mannosyltransferase
  • Dol-P-Man-dependent alpha(1-3)-mannosyltransferase
  • EC 2.4.1.130
  • NOT
  • Not56
  • NOT56LCDG1D
  • Not56-like protein

Background

This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are guaranteed for 3 months from date of receipt.

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Bioinformatics

Gene Symbol ALG3