ALG12 anticorps (N-Term)

N° du produit ABIN5516435

Détail du produit anti-ALG12 anticorps

Antigène: ALG12 (Asparagine-Linked Glycosylation 12, alpha-1,6-Mannosyltransferase Homolog (ALG12))

Épitope: N-Term

Reactivité: Humain, Souris, Rat, Boeuf (Vache), Chien, Chévre, Cobaye, Cheval, Lapin, Saccharomyces cerevisiae, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALG12 est non-conjugé

Application: Western Blotting (WB)

Séquence: EESFNLQATH DLLYHWQDLE QYDHLEFPGV VPRTFLGPVV IAVFSSPAVY

Homologie: Cow: 100%, Dog: 93%, Goat: 79%, Guinea Pig: 93%, Horse: 86%, Human: 100%, Mouse: 100%, Rabbit: 93%, Rat: 100%, Yeast: 85%, Zebrafish: 86%

Attributs du produit: This is a rabbit polyclonal antibody against ALG12. It was validated on Western Blot.

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the N-terminal region of Human ALG12

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur ALG12

Antigène: ALG12 (Asparagine-Linked Glycosylation 12, alpha-1,6-Mannosyltransferase Homolog (ALG12))

Autre désignation: ALG12 (ALG12 Produits)

Sujet: This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation.

Alias Symbols: ALG12, PP14673,

Protein Interaction Partner: RPL13A, PRDX4, UBC,

Protein Size: 488

ID gène: 79087

NCBI Accession: NP_077010

UniProt: Q9BV10