WBSCR16 anticorps (N-Term)

N° du produit ABIN2791205

Détail du produit anti-WBSCR16 anticorps

Antigène: WBSCR16 (Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))

Épitope: N-Term

Reactivité: Humain, Souris, Rat, Porc, Lapin, Boeuf (Vache), Chien, Cobaye, Cheval

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WBSCR16 est non-conjugé

Application: Western Blotting (WB)

Séquence: GYGFTLLSSK TADVTKVWGM GLNKDSQLGF HRSRKDKTRG YEYVLEPSPV

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

Attributs du produit: This is a rabbit polyclonal antibody against WBSCR16. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N-terminal region of Human WBSCR16

Information d'application

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

Commentaires:

Antigen size: 358 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 WBSCR16

Antigène: WBSCR16 (Williams-Beuren Syndrome Chromosome Region 16 (WBSCR16))

Autre désignation: WBSCR16 (WBSCR16 Produits)

Synonymes: anticorps 5730496C04Rik, anticorps AU019812, anticorps RCC1 like, anticorps reculator of chromosome condensation 1 like, anticorps RCC1L, anticorps Rcc1l

Sujet: This gene encodes an RCC1-like G-exchanging factor. It is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Alias Symbols: WBSCR16
Protein Interaction Partner: UBC, NME6, ATXN1, BRCA1, SYNCRIP, HNRNPU, RBBP6, ICT1,
Protein Size: 358

Poids moléculaire: 40 kDa

ID gène: 81554

UniProt: Q8IW88