ALG9 Antibodies

AND ALG9 ELISA kits, ALG9 Proteins

Many biological assays use antibodies to detect ALG9, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with ALG9 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop ALG9 antibodies...

We validate the specificity of these antibodies to ALG9 by testing them on tissues known to express ALG9 positively and negatively. Browse below to find the ALG9 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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ALG9 Infographic by Boster Bio

All ALG9 Products

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ALG9 (NM_024740) Human Over-expression Lysate

Human

$628
Cat # LS079796
100 µg

ALG9 Overview

Facts about Alpha-1,2-mannosyltransferase ALG9.

ALG9 3D structure. Source: alphafold

Alpha-1,2-mannosyltransferase ALG9 (ALG9)

Catalyzes the transfer of mannose from Dol-P-Man into lipid-linked oligosaccharides. .

Gene Information

Human
Gene Name:	ALG9
Uniprot:	Q9H6U8
Entrez:	79796

Family

Belongs to:

glycosyltransferase 22 family

Alternative Names

Alpha-1,2-mannosyltransferase ALG9

Molecular Weight

Mass (kDA):
69.863 kDA

Genomic Context


Human

Location:	11q23.1
Sequence:	11; NC_000011.10 (111776096..111871581, complement)

Tissue Specificity

Ubiquitously expressed; with highest levels in heart, liver and pancreas.

Subcellular Localizations

Endoplasmic reticulum membrane; Multi-pass membrane protein.

Diseases

Congenital disorder of glycosylation 1L (CDG1L)

PTMs

Glycoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/ALG9

References

PMID: 12030331 by Baysal B.E., et al. A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family.

PMID: 15148656 by Frank C.G., et al. Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.