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Probable C-mannosyltransferase

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Probable C-mannosyltransferase that mediates C-mannosylation of tryptophan residues on target proteins.

Below are the list of possible Probable C-mannosyltransferase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Probable C-mannosyltransferase DPY19L1

 Probable C-mannosyltransferase DPY19L1 ELISA Kit
 Probable C-mannosyltransferase DPY19L1 Recombinant
 Probable C-mannosyltransferase DPY19L1 Antibody
Also known as Probable C-mannosyltransferase DPY19L1 (Dpy-19-like protein 1) (Protein dpy-19 homolog 1).
DPY19L1: Belongs to the dpy-19 family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 7p14.3-p14.2

Cellular Component: membrane; nuclear inner membrane

Molecular Function: mannosyltransferase activity

Biological Process: protein amino acid C-linked glycosylation via 2'-alpha-mannosyl-L-tryptophan
 DPY19L1 ELISA Kit
 DPY19L1 Recombinant
 DPY19L1 Antibody
 GA0500 ELISA Kit
 GA0500 Recombinant
 GA0500 Antibody
 KIAA0877 ELISA Kit
 KIAA0877 Recombinant
 KIAA0877 Antibody
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Probable C-mannosyltransferase DPY19L2

 Probable C-mannosyltransferase DPY19L2 ELISA Kit
 Probable C-mannosyltransferase DPY19L2 Recombinant
 Probable C-mannosyltransferase DPY19L2 Antibody
Also known as Probable C-mannosyltransferase DPY19L2 (Dpy-19-like protein 2) (Protein dpy-19 homolog 2).
DPY19L2: Required during spermatogenesis for sperm head elongation and acrosome formation. Defects in DPY19L2 are the cause of spermatogenic failure type 9 (SPGF9). An infertility disorder caused by spermatogenesis defects. The most prominent feature is the malformation of the acrosome, whic
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h can be totally absent in most severe cases. Additional features are an abnormal nuclear shape and abnormal arrangement of the mitochondria of the spermatozoon. Deletions in DPY19L2 are probably the major cause of SPGF9. Belongs to the dpy-19 family.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 12q14.2

Cellular Component: nuclear inner membrane; nucleus

Molecular Function: mannosyltransferase activity

Biological Process: protein amino acid C-linked glycosylation via 2'-alpha-mannosyl-L-tryptophan; spermatid development

Disease: Spermatogenic Failure 9
 DPY19L2 ELISA Kit
 DPY19L2 Recombinant
 DPY19L2 Antibody
 UNQ3127/PRO10284 ELISA Kit
 UNQ3127/PRO10284 Recombinant
 UNQ3127/PRO10284 Antibody
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Probable C-mannosyltransferase DPY19L3

 Probable C-mannosyltransferase DPY19L3 ELISA Kit
 Probable C-mannosyltransferase DPY19L3 Recombinant
 Probable C-mannosyltransferase DPY19L3 Antibody
Also known as Probable C-mannosyltransferase DPY19L3 (Dpy-19-like protein 3) (Protein dpy-19 homolog 3).
DPY19L3: Belongs to the dpy-19 family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 19q13.11

Cellular Component: nuclear inner membrane
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Molecular Function: mannosyltransferase activity

Biological Process: protein amino acid C-linked glycosylation via 2'-alpha-mannosyl-L-tryptophan
 DPY19L3 ELISA Kit
 DPY19L3 Recombinant
 DPY19L3 Antibody
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Probable C-mannosyltransferase DPY19L4

 Probable C-mannosyltransferase DPY19L4 ELISA Kit
 Probable C-mannosyltransferase DPY19L4 Recombinant
 Probable C-mannosyltransferase DPY19L4 Antibody
Also known as Probable C-mannosyltransferase DPY19L4 (Dpy-19-like protein 4) (Protein dpy-19 homolog 4).
DPY19L4: Belongs to the dpy-19 family.

Protein type: Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 8q22.1

Cellular Component: nuclear inner membrane

Molecular Function: mannosyltransferase activity

Biologic
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al Process: protein amino acid C-linked glycosylation via 2'-alpha-mannosyl-L-tryptophan
 DPY19L4 ELISA Kit
 DPY19L4 Recombinant
 DPY19L4 Antibody
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