ALG1 anticorps (N-Term)

N° du produit ABIN2783751

L’anticorps Lapin Polyclonal anti-ALG1 a été validé pour WB. Il convient pour détecter ALG1 dans des échantillons de Humain, Souris, Rat, Lapin, Boeuf (Vache) et Saccharomyces cerevisiae.

Aperçu rapide pour ALG1 anticorps (N-Term) (ABIN2783751)

Antigène: ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))

Reactivité: Humain, Souris, Rat, Lapin, Boeuf (Vache), Saccharomyces cerevisiae

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALG1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ALG1 anticorps

Épitope: N-Term

Séquence: VVLGDVGRSP RMQYHALSLA MHGFSVTLLG FCNSKPHDEL LQNNRIQIVG

Homologie: Cow: 79%, Human: 100%, Mouse: 85%, Rabbit: 79%, Rat: 79%, Yeast: 100%

Attributs du produit: This is a rabbit polyclonal antibody against ALG1. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human ALG1

Information d'application

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

Commentaires:

Antigen size: 464 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

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 ALG1

Antigène: ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))

Autre désignation: ALG1

Sujet: ALG1 catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. Defects in ALG1 are the cause of congenital disorder of glycosylation type 1K (CDG1K).The biosynthesis of lipid-linked oligosaccharides is highly conserved among eukaryotes and is catalyzed by 14 glycosyltransferases in an ordered stepwise manner. Mannosyltransferase I (MT I) catalyzes the first mannosylation step in this process.[supplied by OMIM]. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-421 BM767933.1 1-421 422-1179 AY359073.1 416-1173 1180-1444 CA455103.1 259-523 1445-1939 CD366777.1 17-511 c 1940-2122 BC031095.1 1931-2113 2123-2149 BQ002699.1 1-27 c
Alias Symbols: HMAT1, HMT-1, HMT1, MT-1, CDG1K, Mat-1, hMat-1
Protein Interaction Partner: UBC, FBXO6, BAG3, MMS19,
Protein Size: 464

Poids moléculaire: 52 kDa

ID gène: 56052

NCBI Accession: NM_019109, NP_061982

UniProt: Q9BT22