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Lamin A/C antibody (pSer22)

This anti-Lamin A/C antibody is a Rabbit Polyclonal antibody detecting Lamin A/C in WB and IP. Suitable for Human.
Catalog No. ABIN6136134

Quick Overview for Lamin A/C antibody (pSer22) (ABIN6136134)

Target

See all Lamin A/C (LMNA) Antibodies
Lamin A/C (LMNA)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Lamin A/C antibody is un-conjugated

Application

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Western Blotting (WB), Immunoprecipitation (IP)
  • Binding Specificity

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    pSer22

    Sequence

    PLSPT

    Cross-Reactivity

    Human, Rat

    Characteristics

    Phosphorylated Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic phosphorylated peptide around S22 of human Lamin A (NP_005563.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IP,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Lamin A/C (LMNA)

    Alternative Name

    Lamin A

    Background

    The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants. Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome.,LMNA,CDCD1,CDDC,CMD1A,CMT2B1,EMD2,FPL,FPLD,FPLD2,HGPS,IDC,LDP1,LFP,LGMD1B,LMN1,LMNC,LMNL1,MADA,PRO1,lamin,Lamin A/C,Signal Transduction,PI3K-Akt Signaling Pathway,Cell Biology & Developmental Biology,Apoptosis,Cell Cycle,Cytoskeleton,Intermediate Filaments,Protein folding,Death Receptor Signaling Pathway,Stem Cells,Protein phosphorylation,Lamin A

    Molecular Weight

    62-74 kDa

    Gene ID

    4000

    UniProt

    P02545

    Pathways

    Apoptosis, Caspase Cascade in Apoptosis, ER-Nucleus Signaling, Protein targeting to Nucleus
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