ALG9 Antibody | 16-885

ALG9 Antibody | 16-885 | Gentaur UK, US & Europe Distribution

Host: Rabbit

Reactivity: Human

Homology: N/A

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 439-618 of human ALG9 (NP_079016.2) .

Research Area: Other

Tested Application: WB

Application: WB: 1:500 - 1:2000

Specificiy: N/A

Positive Control 1: N/A

Positive Control 2: N/A

Positive Control 3: N/A

Positive Control 4: N/A

Positive Control 5: N/A

Positive Control 6: N/A

Molecular Weight: N/A

Validation: N/A

Isoform: N/A

Purification: Affinity purification

Clonality: Polyclonal

Clone: N/A

Isotype: IgG

Conjugate: Unconjugated

Physical State: Liquid

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Concentration: N/A

Storage Condition: Store at -20˚C. Avoid freeze / thaw cycles.

Alternate Name: CDG1L, DIBD1, GIKANIS, LOH11CR1J, alpha-1, 2-mannosyltransferase ALG9, asparagine-linked glycosylation 9 alpha-12-mannosyltransferase-like protein, asparagine-linked glycosylation 9 homolog (S. cerevisiae, alpha- 1, 2-mannosyltransferase) , asparagine-linked glycosylation 9 homolog (yeast, alpha- 1, 2-mannosyltransferase) , asparagine-linked glycosylation 9, alpha-1, 2-mannosyltransferase homolog, asparagine-linked glycosylation protein 9 homolog, disrupted in bipolar affective disorder 1, disrupted in bipolar disorder protein 1, dol-P-Man dependent alpha-1, 2-mannosyltransferase, dol-P-Man:Man (6) GlcNAc (2) -PP-Dol alpha-1, 2-mannosyltransferase, dol-P-Man:Man (8) GlcNAc (2) -PP-Dol alpha-1, 2-mannosyltransferase, dolichyl-P-Man:Man (6) GlcNAc (2) -PP-dolichol alpha-1, 2-mannosyltransferase, dolichyl-P-Man:Man (8) GlcNAc (2) -PP-dolichol alpha-1, 2-mannosyltransferase, loss of heterozygosity, 11, chromosomal region 1 gene J product

User Note: Optimal dilutions for each application to be determined by the researcher.

BACKGROUND: This gene encodes an alpha-1, 2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene.