WDR35 anticorps (AA 871-1170)

N° du produit ABIN6150192

L’anticorps Lapin Polyclonal anti-WDR35 a été validé pour WB et IF. Il convient pour détecter WDR35 dans des échantillons de Humain.

Aperçu rapide pour WDR35 anticorps (AA 871-1170) (ABIN6150192)

Antigène: WDR35 (WD Repeat Domain 35 (WDR35))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WDR35 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Détail du produit anti-WDR35 anticorps

Épitope: AA 871-1170

Séquence: CSQPKAAVDT CVHLNQWNKA VELAKNHSMK EIGSLLARYA SHLLEKNKTL DAIELYRKAN YFFDAAKLMF KIADEEAKKG SKPLRVKKLY VLSALLIEQY HEQMKNAQRG KVKGKSSEAT SALAGLLEEE VLSTTDRFTD NAWRGAEAYH FFILAQRQLY EGCVDTALKT ALHLKDYEDI IPPVEIYSLL ALCACASRAF GTCSKAFIKL KSLETLSSEQ KQQYEDLALE IFTKHTSKDN RKPELDSLME GGEGKLPTCV ATGSPITEYQ FWMCSVCKHG VLAQEISHYS FCPLCHSPVG

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 871-1170 of human WDR35 (NP_065830.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:1000,IF,1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

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

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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur WDR35

Antigène: WDR35 (WD Repeat Domain 35 (WDR35))

Autre désignation: WDR35

Sujet: This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Two patients with Sensenbrenner syndrome / cranioectodermal dysplasia (CED) were identified with mutations in this gene, consistent with a possible ciliary function.,WDR35,CED2,IFT121,IFTA1,SRTD7,Cell Biology & Developmental Biology,WDR35

Poids moléculaire: 132 kDa/133 kDa

ID gène: 57539

UniProt: Q9P2L0

Pathways: Signalisation Hedgehog