NPHP3 Antikörper (AA 1-130)

Produktnummer ABIN6144770

Produktdetails anti-NPHP3 Antikörper

Target: NPHP3 (Nephronophthisis 3 (Adolescent) (NPHP3))

Bindungsspezifität: AA 1-130

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NPHP3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MGTASSLVSP AGGEVIEDTY GAGGGEACEI PVEVKPKARL LRNSFRRGAG AAAGAGPGSL PRGVGAGGLL GASFKSTGSS VPELEYAAAE YERLRKEYEI FRVSKNQELL SMGRREAKLD TENKRLRAEL

Kreuzreaktivität: Human, Maus

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-130 of human NPHP3 (NP_694972.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:200 - 1:2000

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 NPHP3

Target: NPHP3 (Nephronophthisis 3 (Adolescent) (NPHP3))

Andere Bezeichnung: NPHP3 (NPHP3 Produkte)

Synonyme: si:dkey-56l10.1 antikoerper, MKS7 antikoerper, NPH3 antikoerper, RHPD antikoerper, 3632410F03Rik antikoerper, AI550417 antikoerper, C230078J01 antikoerper, D330020E01Rik antikoerper, pcy antikoerper, RGD1563856 antikoerper, nephronophthisis 3 antikoerper, nephrocystin 3 antikoerper, nephronophthisis 3 (adolescent) antikoerper, nphp3 antikoerper, NPHP3 antikoerper, Nphp3 antikoerper

Hintergrund: This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene.,NPHP3,CFAP31,MKS7,NPH3,RHPD,RHPD1,SLSN3,NPHP3

Molekulargewicht: 15 kDa/19 kDa/26 kDa/71 kDa/73 kDa/79 kDa/150 kDa

Gen-ID: 27031

UniProt: Q7Z494

Pathways: cAMP Metabolic Process