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ALG9 Polyclonal Antibody

CAT: 0763-E-AB-10773-02Size: 60 µLDry Ice: NoHazardous: No
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CAT#:0763-E-AB-10773-02Size:60 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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.
Abbreviation
ALG9
UniProt
Q9H6U8
Host
Rabbit
Reactivity
Human; Mouse
Immunogen
Recombinant protein of human ALG9
Target
ALG9; ALG9; Alpha-1;2-mannosyltransferase ALG9; Asparagine-linked glycosylation protein 9 homolog; Disrupted in bipolar disorder protein 1
Clonality
Polyclonal
Conjugation
Unconjugated
Applications
IHC
Purification
Affinity purification
Concentration
0.3 mg/mL
Dilution
IHC 1:50-1:200
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Shipping Conditions
The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.
Storage Conditions
Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Isotype
IgG

UniProtKB · Q9H6U8

Alpha-1,2-mannosyltransferase ALG9

ALG9_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9H6U8
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ALG9
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.4.1.259, 2.4.1.261
Processing
—
Secondary accessions
Q6ZMD5, Q7Z4R4, Q96GS7, Q96PB9, Q9H068
Protein keywords

Coding sequence diversity

Alternative splicingChromosomal rearrangement

Disease

Congenital disorder of glycosylationDisease variant

Cellular component

Endoplasmic reticulumMembrane

PTM

Glycoprotein

Molecular function

GlycosyltransferaseTransferase

Technical term

Proteomics identificationReference proteome

Domain

TransmembraneTransmembrane helix

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