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Anti-Phospho-Lamin A/C (Ser22) Rabbit pAb

Purified Rabbit Polyclonal Antibody

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货号 规格 价格
P108482
20µL ¥588.00
50µL ¥1080.00
100µL ¥1780.00

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Anti-Phospho-Lamin A/C (Ser22) Rabbit pAb
Anti-Phospho-Lamin A/C (Ser22) Rabbit pAb
Product NameAnti-Phospho-Lamin A/C (Ser22) Rabbit pAb
DescriptionPurified Rabbit Polyclonal Antibody
Application
  • Applications Legend:
  • WB=Western Blotting
  • IHC-P=Immunohistochemistry (Paraffin)
  • IHC-F=Immunohistochemistry (Frozen)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IP, ELISA
DilutionWB 1:500~1:2,000; IP 0.5μg-4μg antibody for 200μg-400μg extracts of whole cells
ReactivityHuman, Rat
HostRabbit
ClonalityPolyclonal
IsotypeIgG
LabelUnconjugated
ImmunogenA synthetic phosphorylated peptide around S22 of human Lamin A (NP_005563.1).
FormatAffinity purified polyclonal antibody supplied in PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
SynonymsFPL; IDC; LFP; CDDC; EMD2; FPLD; HGPS; LDP1; LMN1; LMNC; MADA; PRO1; CDCD1; CMD1A; FPLD2; LMNL1; CMT2B1; LGMD1B; Phospho-Lamin A/C-S22.
Molecular weightCalculated MW: 74 kDa; Observed MW: 69 kDa, 78 kDa
Uniprot ID P02545
Gene ID 4000
StorageShipped on wet ice. Store at -20℃. Stable for 24 months from date of receipt. Aliquoting is unnecessary for -20℃ storage.
PrecautionsAnti-Phospho-Lamin A/C (Ser22) Rabbit pAb is for research use only and not for use in diagnostic or therapeutic procedures.
Background The protein encoded by this gene is part of the nuclear lamina, 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.

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