ALG3 Antibody

Code CSB-PA846090XA01HU
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) ALG3 Polyclonal antibody
Uniprot No.
Target Names
ALG3
Alternative Names
ALG3 antibody; NOT antibody; NOT56LDol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase antibody; EC 2.4.1.258 antibody; Asparagine-linked glycosylation protein 3 homolog antibody; Dol-P-Man-dependent alpha(1-3)-mannosyltransferase antibody; Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase antibody; Dolichyl-phosphate-mannose--glycolipid alpha-mannosyltransferase antibody; Not56-like protein antibody
Raised in
Rabbit
Species Reactivity
Homo sapiens (Human)
Immunogen
Recombinant Homo sapiens (Human) ALG3 protein
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, WB (ensure identification of antigen)
Protocols
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Value-added Deliverables
① 200ug * antigen (positive control);
② 1ml * Pre-immune serum (negative control);
Quality Guarantee
① Antibody purity can be guaranteed above 90% by SDS-PAGE detection;
② ELISA titer can be guaranteed 1: 64,000;
③ WB validation with antigen can be guaranteed positive;
Lead Time
Made-to-order (14-16 weeks)
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Adds the first Dol-P-Man derived mannose in an alpha-1,3 linkage to Man5GlcNAc2-PP-Dol.
Gene References into Functions
  1. Silencing ALG3 or HSF2 inhibited the proliferation, migration, and invasion abilities of MCF-7 cells. PMID: 29799832
  2. ALG3-CDG is due to an autosomal recessive defect in the ER mannosyl-transferase VI, which is involved in protein N-glycosylation. The enzyme is encoded by the ALG3 gene PMID: 23791010
  3. a mutation in ALG3 affects splicing and may have a role in development of congenital disorder of glycosylation type Id [case report] PMID: 16006436
Involvement in disease
Congenital disorder of glycosylation 1D (CDG1D)
Subcellular Location
Endoplasmic reticulum membrane; Multi-pass membrane protein.
Protein Families
Glycosyltransferase 58 family
Database Links

HGNC: 23056

OMIM: 601110

KEGG: hsa:10195

STRING: 9606.ENSP00000380793

UniGene: Hs.478481

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301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
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Address
7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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