BBS5 anticorps (Middle Region)

N° du produit ABIN2774032

Détail du produit anti-BBS5 anticorps

Antigène: BBS5 (Bardet-Biedl Syndrome 5 (BBS5))

Épitope: Middle Region

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

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BBS5 est non-conjugé

Application: Western Blotting (WB)

Séquence: VEIDSDGHTD AFVAYFADGN KQQDREPVFS EELGLAIEKL KDGFTLQGLW

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

Attributs du produit: This is a rabbit polyclonal antibody against BBS5. 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 middle region of human BBS5

Information d'application

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

Commentaires:

Antigen size: 341 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 BBS5

Antigène: BBS5 (Bardet-Biedl Syndrome 5 (BBS5))

Autre désignation: BBS5 (BBS5 Produits)

Synonymes: anticorps zgc:56578, anticorps 1700049I01Rik, anticorps 2700023J09Rik, anticorps Bardet-Biedl syndrome 5, anticorps Bardet-Biedl syndrome 5 (human), anticorps bbs5, anticorps BBS5, anticorps Bbs5

Sujet: BBS5 is a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia.This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized.
Alias Symbols: -
Protein Interaction Partner: KLC3, CRADD,
Protein Size: 341

Poids moléculaire: 39 kDa

ID gène: 129880

NCBI Accession: NM_152384, NP_689597

UniProt: Q8N3I7

Pathways: Signalisation Hedgehog