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ALG2 Products

(Asparagine-Linked Glycosylation 2, alpha-1,3-Mannosyltransferase Homolog (ALG2))

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This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diphosphate. Defects in this gene have been associated with congenital disorder of glycosylation type Ih (CDG-Ii). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008].

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Featured ALG2 Categories

ALG2 Antibodies

High quality antibodies with extensive validation data.

ALG2 Proteins

Proteins for various applications incl. WB, ELISA, IF etc.

Recommended ALG2 Antibodies

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Application ELISA, IHC, IF
Validations
  • (3)
Cat. No. ABIN7143770
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application WB
Validations
  • (3)
Cat. No. ABIN949751
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application ELISA, IHC
Validations
  • (2)
Cat. No. ABIN7143769
Quantity 100 μL
Datasheet Datasheet

Recommended ALG2 Proteins

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source Wheat germ
Validations
  • (1)
Cat. No. ABIN1344874
Quantity 10 μg
Datasheet Datasheet
Reactivity Human
Source Wheat germ
Validations
  • (1)
Cat. No. ABIN1344876
Quantity 10 μg
Datasheet Datasheet
Reactivity Human
Source Tobacco (Nicotiana tabacum)
Validations
Cat. No. ABIN3106782
Quantity 1 mg
Datasheet Datasheet

Latest Publications for our ALG2 products

Cossins, Belaya, Hicks, Salih, Finlayson, Carboni, Liu, Maxwell, Zoltowska, Farsani, Laval, Seidhamed, Donnelly, Bentley, McGowan, Müller, Palace, Lochmüller, Beeson: "Congenital myasthenic syndromes due to mutations in ALG2 and ALG14." in: Brain : a journal of neurology, Vol. 136, Issue Pt 3, pp. 944-56, (2013) (PubMed).

Rind, Schmeiser, Thiel, Absmanner, Lübbehusen, Hocks, Apeshiotis, Wilichowski, Lehle, Körner: "A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." in: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).

Synonyms and alternative names related to ALG2

ALG2, alpha-1,3/1,6-mannosyltransferase (ALG2), asparagine-linked glycosylation 2 (alpha-1,3-mannosyltransferase) (Alg2), ALG2, alpha-1,3/1,6-mannosyltransferase (Alg2), ALG2, alpha-1,3/1,6-mannosyltransferase L homeolog (alg2.L), GDP-Man:Man(1)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase (ALG2), asparagine-linked glycosylation 2 (alpha-1,3-mannosyltransferase) (alg2), 1110018A23Rik, 1300013N08Rik, ALPG2, CDGIi, hALPG2, im:7145131, MNCb-5081, NET38

Protein level used designations for ALG2

  • GDP-Man:Man(1)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase
  • GDP-Man:Man(1)GlcNAc(2)-PP-dolichol mannosyltransferase
  • GDP-Man:Man(2)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase
  • alpha-1,3-mannosyltransferase ALG2
  • alpha-1,3/1,6-mannosyltransferase ALG2
  • asparagine-linked glycosylation 2 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase)
  • asparagine-linked glycosylation 2 homolog (yeast, alpha-1,3-mannosyltransferase)
  • asparagine-linked glycosylation 2, alpha-1,3-mannosyltransferase homolog
  • asparagine-linked glycosylation protein 2 homolog
  • homolog of yeast ALG2
  • hypothetical protein
  • LOW QUALITY PROTEIN: alpha-1,3/1,6-mannosyltransferase ALG2
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