Lamin A/C (Phospho Ser392) (PTR1133) Mouse mAb

-YP1876

Catalog: YP1876
Size
Price
Status
Qty.
200μL
$936.00
3 weeks

0

100μL
$560.00
3 weeks

0

50μL
$300.00
3 weeks

0

Add to cart

Collected

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Main Information
Target

Lamin A/C (phospho Ser392) Phospho Ser392

Host Species

Mouse

Reactivity

Human, Mouse, Rat, Monkey

Applications

WB, IHC, IF, ELISA

MW

63kD,74kD (Calculated)

63kD,74kD (Observed)

Conjugate/Modification


phosphate

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; IHC 1:200-1:1000; IF 1:100-500; ELISA 1:1000-5000
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
This antibody detects endogenous levels of Lamin A/C (phospho Ser392) protein.
Purification
Recombinant Antibody  expressed in animal component-free (ACF) media, purified via Protein G affinity chromatography.
Storage
-15°C to -25°C/1 year (Do not lower than -25°C)
Concentration
1 mg/ml
MW(Calculated)
63kD,74kD
MW(Observed)
63kD,74kD
Modification
phosphate
Clonality
Monoclonal
Clone Number
PTR1133
Isotype
IgG1, Kappa
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ELISA Kits
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human protein. AA range: 350-450
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Specificity:
This antibody detects endogenous levels of Lamin A/C (phospho Ser392) protein.
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Gene Name:
LMNA LMN1
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Protein Name:
Prelamin-A/C [Cleaved into: Lamin-A/C (70 kDa lamin) (Renal carcinoma antigen NY-REN-32) ]
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Other Name:
Prelamin-A/C [Cleaved into: Lamin-A/C ;
70 kDa lamin ;
Renal carcinoma antigen NY-REN-32 ;
]
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Database Link:
Organism Gene ID SwissProt
Human 4000; P02545;
Mouse 16905; P48678;
Rat 60374; P48679;
Background:
lamin A/C (LMNA) Homo sapiens 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. [provided by RefSeq , Apr 2012] ,
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Function:
Lamins are components of the nuclear lamina , a fibrous layer on the nucleoplasmic side of the inner nuclear membrane , which is thought to provide a framework for the nuclear envelope and may also interact with chromatin. Lamin A and C are present in equal amounts in the lamina of mammals. Recruited by DNA repair proteins XRCC4 and IFFO1 to the DNA double-strand breaks (DSBs) to prevent chromosome translocation by immobilizing broken DNA ends . Plays an important role in nuclear assembly , chromatin organization , nuclear membrane and telomere dynamics. Required for normal development of peripheral nervous system and skeletal muscle and for muscle satellite cell proliferation . Required for osteoblastogenesis and bone formation . Also prevents fat infiltration of muscle and bone marrow , helping to maintain the volume and strength of skeletal muscle and bone . Required for cardiac homeostasis . ; Prelamin-A/C can accelerate smooth muscle cell senescence. It acts to disrupt mitosis and induce DNA damage in vascular smooth muscle cells (VSMCs) , leading to mitotic failure , genomic instability , and premature senescence.
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Catalog: YP1876
Size
Price
Status
Qty.
200μL
$936.00
3 weeks

0

100μL
$560.00
3 weeks

0

50μL
$300.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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