DYNC2H1 Antikörper

Produktnummer ABIN6567791

Produktdetails anti-DYNC2H1 Antikörper

Target: DYNC2H1 (Dynein, Cytoplasmic 2, Heavy Chain 1 (DYNC2H1))

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DYNC2H1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant Protein of human DYNC2H1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1 mg/mL

Buffer: 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 DYNC2H1

Target: DYNC2H1 (Dynein, Cytoplasmic 2, Heavy Chain 1 (DYNC2H1))

Andere Bezeichnung: DYNC2H1 (DYNC2H1 Produkte)

Synonyme: dhc2 antikoerper, dhc1b antikoerper, dnch2 antikoerper, dyh1b antikoerper, 4432416O06Rik antikoerper, AI448217 antikoerper, D030010H02Rik antikoerper, D330044F14Rik antikoerper, DHC1b antikoerper, DHC2 antikoerper, Dnchc2 antikoerper, b2b414Clo antikoerper, mKIAA1997 antikoerper, Dnch2 antikoerper, ATD3 antikoerper, DNCH2 antikoerper, DYH1B antikoerper, SRPS2B antikoerper, hdhc11 antikoerper, dynein cytoplasmic 2 heavy chain 1 antikoerper, dynein, cytoplasmic 2, heavy chain 1 antikoerper, cytoplasmic dynein 1b heavy chain antikoerper, DYNC2H1 antikoerper, dync2h1 antikoerper, DHC1b antikoerper, Dync2h1 antikoerper

Hintergrund:

Synonyms: Cytoplasmic dynein 2 heavy chain 1,Cytoplasmic dynein 2 heavy chain,DYHC2,DYNC2H1,Dynein cytoplasmic heavy chain 2,Dynein heavy chain 11,Dynein heavy chain isotype 1B,hDHC11

Background: This gene encodes a large cytoplasmic dynein protein that is involved in retrograde transport in the cilium and has a role in intraflagellar transport, a process required for ciliary/flagellar assembly. Mutations in this gene cause a heterogeneous spectrum of conditions related to altered primary cilium function and often involve polydactyly, abnormal skeletogenesis, and polycystic kidneys. Alternative splicing results in multiple transcript variants encoding distinct proteins.

Molekulargewicht:

Observed_MW: 493kDa

Calculated_MW: 105kDa/492kDa/493kDa

Gen-ID: 79659

UniProt: Q8NCM8

Pathways: Hedgehog Signalweg, Asymmetric Protein Localization