BBS10 Antikörper (AA 474-723)

Produktnummer ABIN6137466

Produktdetails anti-BBS10 Antikörper

Target: BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

Bindungsspezifität: AA 474-723

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BBS10 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: AENKDALEKT QTYLKVHSNL VIPDVELETY IPYSTPTLTP TDTFQTVETL TCLSLERNRL TDYYEPLLKN NSTAYSTRGN RIEISYENLQ VTNITRKGSM LPVSCKLPNM GTSQSYLSSS MPAGCVLPVG GNFEILLHYY LLNYAKKCHQ SEETMVSMII ANALLGIPKV LYKSKTGKYS FPHTYIRAVH ALQTNQPLVS SQTGLESVMG KYQLLTSVLQ CLTKILTIDM VITVKRHPQK VHNQDSEDEL

Kreuzreaktivität: Human, Maus

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 474-723 of human BBS10 (NP_078961.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:200 - 1:3000

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu BBS10

Target: BBS10 (Bardet-Biedl Syndrome 10 (BBS10))

Andere Bezeichnung: BBS10 (BBS10 Produkte)

Synonyme: MGC84945 antikoerper, si:dkey-30c15.16 antikoerper, C12orf58 antikoerper, RGD1560748 antikoerper, 1300007O09Rik antikoerper, AI452285 antikoerper, Bardet-Biedl syndrome 10 antikoerper, Bardet-Biedl syndrome 10 L homeolog antikoerper, Bardet-Biedl syndrome 10 (human) antikoerper, BBS10 antikoerper, bbs10.L antikoerper, bbs10 antikoerper, Bbs10 antikoerper

Hintergrund: This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, 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 is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10.,BBS10,C12orf58,Epigenetics & Nuclear Signaling,Transcription Factors,Neuroscience,BBS10

Molekulargewicht: 80 kDa

Gen-ID: 79738

UniProt: Q8TAM1