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N-Myc Downstream Regulated 1 (NDRG1) Peptid

NDRG1 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN980553

Kurzübersicht für N-Myc Downstream Regulated 1 (NDRG1) Peptid (ABIN980553)

Target

NDRG1 (N-Myc Downstream Regulated 1 (NDRG1))

Spezies

Human

Quelle

  • 6
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Produktmerkmale

    This is a synthetic peptide designed for use in combination with anti-NDRG1 antibody (Catalog #: ARP47974_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Aufreinigung

    Purified
  • Applikationshinweise

    Each Investigator should determine their own optimal working dilution for specific applications.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    NDRG1 (N-Myc Downstream Regulated 1 (NDRG1))

    Hintergrund

    NDRG1 is a member of the N-myc downregulated protein family which belongs to the alpha/beta hydrolase superfamily. NDRG1 is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. Mutation in its gene has been reported to be causative for hereditary motor and sensory neuropathy-Lom.This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. Mutation in this gene has been reported to be causative for hereditary motor and sensory neuropathy-Lom.

    Alias Symbols: CAP43, CMT4D, DRG1, GC4, HMSNL, NDR1, NMSL, PROXY1, RIT42, RTP, TARG1, TDD5

    Protein Interaction Partner: ACSL3,ACTG1,AP1M2,AP2M1,ARL4D,ATP1A1,CANX,CDH1,CLTC,CNDP2,COPB2,CTNNB1,DDX1,DDX5,DLST,EEF1G,EEF2,EIF2S3,EIF3E,EWSR1,FASN,HNRNPF,HNRNPH1,HNRNPU,HSD17B4,HSP90AA1,HSPA5,ILF3,KIF5B,LDHA,MAOA,MME,NCL,PABPC1,PHYHIP,PKM2,PPP2R2A,PRKACA,PSMC2,PSMC3,PSMD2,RPL24,RPL3,RPL4,RPN2,RPS16,RPS20,RPS26,RPS3,RPS6,RPS8,RUVBL2,S100B,SEC23A,SHMT2,TARS,TLE3,UPF1,VCP,XRCC5,ZNF155,ARL4D,PHYHIP,S100B

    Protein Size: 394

    Molekulargewicht

    43 kDa

    Gen-ID

    10397

    NCBI Accession

    NM_006096, NP_006087

    UniProt

    Q92597
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