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ALG2 Antibody

CAT: 0013-GTR17907780-02Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR17907780-02Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
This ALG2 Antibody is an unconjugated polyclonal product. It tagets ALG2 using a Recombinant Human Alpha-1,3/1,6-mannosyltransferase ALG2 protein (303-405AA) as the immunogen. This antibody is suitable for ELISA, IF, IHC. Purification: >95%, Protein G purified.
Product Name Alternative
3-mannosyltransferase ALG2 antibody; ALG2 alpha-1,3/1,6-mannosyltransferase antibody; ALG2 antibody; ALG2_HUMAN antibody; Alpha 1,3 mannosyltransferase ALG2 antibody; Alpha-1 antibody; Asparagine linked glycosylation protein 2 antibody; Asparagine-linked glycosylation protein 2 homolog antibody; CDGIi antibody; FLJ14511 antibody; GDP Man:Man (1) GlcNAc (2) PP dolichol mannosyltransferase antibody; GDP-Man:Man (1) GlcNAc (2) -PP-dolichol mannosyltransferase antibody; hALPG2 antibody; NET38 antibody; OTTHUMP00000021785 antibody; OTTHUMP00000123474 antibody; RP11-13B9.1 antibody
UniProt
Q9H553
Reactivity
Human
Immunogen
Recombinant Human Alpha-1,3/1,6-mannosyltransferase ALG2 protein (303-405AA)
Target
ALG2
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Cell Biology
Purification
>95%, Protein G purified
Dilution
IHC-P:1:20-200, IF:1:50-200
Form
Liquid
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
ELISA, IF, IHC
Host or Source
Rabbit
Preservative
Preservative: 0.03% Proclin 300. Constituents: 50% Glycerol
Isotype
IgG

UniProtKB · Q9H553

Alpha-1,3/1,6-mannosyltransferase ALG2

ALG2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9H553
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ALG2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.4.1.132, 2.4.1.257
Processing
—
Secondary accessions
A2A2Y0, Q8NBX2, Q8NC39
Protein keywords

Coding sequence diversity

Alternative splicing

Disease

Congenital disorder of glycosylationCongenital myasthenic syndromeDisease variant

Cellular component

Endoplasmic reticulumMembrane

Molecular function

GlycosyltransferaseTransferase

Technical term

Proteomics identificationReference proteome

Domain

TransmembraneTransmembrane helix

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