BBS2 anticorps (N-Term)

N° du produit ABIN2788195

Cet anticorps Lapin Polyclonal détecte spécifiquement BBS2 dans WB. Il présente une réactivité envers Humain, Souris, Rat, Chien, Boeuf (Vache), Cheval, Lapin, Poisson zèbre (Danio rerio) et Cobaye.

Aperçu rapide pour BBS2 anticorps (N-Term) (ABIN2788195)

Antigène: BBS2 (Bardet-Biedl Syndrome 2 (BBS2))

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BBS2 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-BBS2 anticorps

Épitope: N-Term

Séquence: GSDLFWTVTG DNVNSLALCD FDGDGKKELL VGSEDFDIRV FKEDEIVAEM

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

Attributs du produit: This is a rabbit polyclonal antibody against BBS2. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human BBS2

Information d'application

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

Commentaires:

Antigen size: 721 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 BBS2

Antigène: BBS2 (Bardet-Biedl Syndrome 2 (BBS2))

Autre désignation: BBS2

Sujet: This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with six other BBS proteins.
Alias Symbols: BBS, MGC20703
Protein Interaction Partner: PSME3, MDFI, RBPMS, GLIS2, HSCB, FHOD1, EXOC7, PAX2, KRT18, EPAS1, EEF1A1, BHMT, ALDOB, UBC, UBD,
Protein Size: 721

Poids moléculaire: 80 kDa

ID gène: 583

NCBI Accession: NM_031885, NP_114091

UniProt: Q9BXC9

Pathways: Signalisation Hedgehog