B9D1 anticorps (N-Term)

N° du produit ABIN2790914

L’anticorps Lapin Polyclonal anti-B9D1 a été validé pour WB. Il convient pour détecter B9D1 dans des échantillons de Humain, Souris, Rat, Boeuf (Vache), Chien, Cobaye, Cheval et Lapin.

Aperçu rapide pour B9D1 anticorps (N-Term) (ABIN2790914)

Antigène: B9D1 (B9 Protein Domain 1 (B9D1))

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp B9D1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-B9D1 anticorps

Épitope: N-Term

Séquence: VYGQDWAPTA GLEEGISQIT SKSQDVRQAL VWNFPIDVTF KSTNPYGWPQ

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

Attributs du produit: This is a rabbit polyclonal antibody against B9D1. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N-terminal region of Human B9D1

Information d'application

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

Commentaires:

Antigen size: 204 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 B9D1

Antigène: B9D1 (B9 Protein Domain 1 (B9D1))

Autre désignation: B9D1

Sujet: This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Three alternatively spliced transcript variants that encode different proteins have been described for this gene.
Alias Symbols: B9, EPPB9, MKS9, MKSR1
Protein Interaction Partner: EXOSC10, UBC, LIG4,
Protein Size: 204

Poids moléculaire: 22 kDa

ID gène: 27077

NCBI Accession: NM_015681, NP_056496

UniProt: Q9UPM9