ALG11 Polyclonal Antibody
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


ALG11 Polyclonal Antibody
Background:
Mannosyltransferase involved in the last steps of the synthesis of Man5GlcNAc (2) -PP-dolichol core oligosaccharide on the cytoplasmic face of the endoplasmic reticulum. Catalyzes the addition of the 4th and 5th mannose residues to the dolichol-linked oligosaccharide chain.Involvement in disease:Defects in ALG11 are the cause of congenital disorder of glycosylation type 1P (CDG1P) . A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.Synonyms:
Asparagine-linked glycosylation protein 11 homolog; AI849156; alg11; ALG11_HUMAN; Asparagine-linked glycosylation 11; Asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase homolog yeast; GT8; UTP14C.Gene ID:
440138Cellular Locus:
Cytoplasm, Cell membraneHost:
RabbitImmunogen:
301-385/492Target:
ALG11Clonality:
PolyclonalIsotype:
IgGConjugation:
UnconjugatedSource:
KLH conjugated synthetic peptide derived from human ALG11Applications:
ELISA, IHC-P, IHC-F, IF (IHC-P), IF (IHC-F), IF (ICC)Purification:
Purified by Protein A.Concentration:
1µg/µlDilution:
ELISA (1:500-1000), IHC-P (1:200-400), IHC-F (1:100-500), IF (IHC-P) (1:50-200), IF (IHC-F) (1:50-200), IF (ICC) (1:50-200)Buffer:
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.Modification:
UnmodifiedStorage Conditions:
Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.Gene ID URL:
440138Predicted Cross Reactivity:
Human, Mouse, Rat, Dog, Horse
