KD-Validated Lamin A/C Recombinant Rabbit Monoclonal Antibody
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,ICC

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Gene Name:LMNA
SKU: KVAb01348
Detail

Summary

Production Name

KD-Validated Lamin A/C Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,FCM,ICC

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

LMNA

Alternative Names

LMNA; Lamin A/C; HGPS; MADA; LMN1; Mandibuloacral Dysplasia Type A; Lamin A/C-Like 1; Prelamin-A/C; Progerin; LGMD1B; CMD1A; LMNL1; PRO1; Limb Girdle Muscular Dystrophy 1B (Autosomal Dominant); Cardiomyopathy, Dilated 1A (Autosomal Dominant); Epididymis Secretory Sperm Binding Protein; Progeria 1 (Hutchinson-Gilford Type); Renal Carcinoma Antigen NY-REN-32; 70 KDa Lamin; Lamin C; CMT2B1; CDCD1; FPLD2; Lamin; CDDC; EMD2; FPLD; LDP1; LMNC; FPL; IDC; LFP

Gene ID

4000

SwissProt ID

P02545

 

Application

Dilution Ratio

WB 1:1,000-1:5,000; FC 1:200-1:2,000; ICC 1:100-1:1,000

Molecular Weight

Calculated MW: 74.1kDa

 

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. [provided by RefSeq, May 2022]

 

Research Area

Tags & Cell Markers,Signal Transduction

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