ALG12 anticorps (N-Term)

N° du produit ABIN5516435

Cet anticorps anti-ALG12 est un anticorps Lapin Polyclonal détectant ALG12 dans WB. Adapté pour Humain, Souris, Rat, Boeuf (Vache), Chien, Chévre, Cobaye, Cheval, Lapin, Saccharomyces cerevisiae et Poisson zèbre (Danio rerio).

Aperçu rapide pour ALG12 anticorps (N-Term) (ABIN5516435)

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

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)

Détail du produit anti-ALG12 anticorps

Épitope: N-Term

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

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