Lamin B Receptor anticorps (AA 1-211)

N° du produit ABIN6143105

Détail du produit anti-Lamin B Receptor anticorps

Antigène: Lamin B Receptor (LBR)

Épitope: AA 1-211

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Lamin B Receptor est non-conjugé

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

Séquence: MPSRKFADGE VVRGRWPGSS LYYEVEILSH DSTSQLYTVK YKDGTELELK ENDIKPLTSF RQRKGGSTSS SPSRRRGSRS RSRSRSPGRP PKSARRSASA SHQADIKEAR REVEVKLTPL ILKPFGNSIS RYNGEPEHIE RNDAPHKNTQ EKFSLSQESS YIATQYSLRP RREEVKLKEI DSKEEKYVAK ELAVRTFEVT PIRAKDLEFG G

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-211 of human LBR (NP_002287.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IF,1:50 - 1:100

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 Lamin B Receptor

Antigène: Lamin B Receptor (LBR)

Autre désignation: LBR (LBR Produits)

Synonymes: anticorps CG17952, anticorps Dmel\\CG17952, anticorps dLBR, anticorps sb:cb406, anticorps zgc:86649, anticorps wu:fb75h08, anticorps wu:fc47b04, anticorps wu:fd36b07, anticorps lbr-A, anticorps Xp58, anticorps p58 gene, anticorps LBR, anticorps DHCR14B, anticorps LMN2R, anticorps PHA, anticorps TDRD18, anticorps AI505894, anticorps ic, anticorps Nbp60, anticorps lamin B receptor, anticorps Lamin B receptor, anticorps lamin B receptor S homeolog, anticorps LBR, anticorps lbr, anticorps lbr.S, anticorps Lbr

Sujet: The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified.,LBR,DHCR14B,LMN2R,PHA,TDRD18,Epigenetics & Nuclear Signaling,Cancer,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Intermediate Filaments,Endocrine & Metabolism,Lipid Metabolism,LBR

Poids moléculaire: 70 kDa

ID gène: 3930

UniProt: Q14739