PIMA535618

Lamin B2 Recombinant Rabbit Monoclonal Antibody (ARC1252), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIMA535618-Each-of-1 In Stock ₹ 49,172.50

PIMA535618 - Each of 1

₹ 49,172.50

In Stock

Quantity

1

Base Price: ₹ 49,172.50

GST (18%): ₹ 8,851.05

Total Price: ₹ 58,023.55

Antigen

Lamin B2

Classification

Monoclonal

Concentration

0.2 mg/mL

Formulation

PBS with 0.05% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3

Gene Accession No.

P21619, Q03252

Gene Symbols

LMNB2

Immunogen

A synthetic peptide corresponding to a sequence within amino acids 521-620 of human Lamin B2 (Q03252)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Clone

ARC1252

Conjugate

Unconjugated

Gene

LMNB2

Gene Alias

EPM9; fc15d06; im:7142331; LAMB2; lamin; lamin A/C; lamin B2; lamin B2 S homeolog; lamin B3; lamin-B2; Lamin-L(II); LMN2; LMNA; lmnb2; lmnb2.S; lmnb2-a; lmnb2-b; MGC2721; RGD1563803; unnamed protein product; wu:fb94e05; wu:fb95e12; wu:fc15d06; wu:fc49h03; XELAEV_18009631mg

Host Species

Rabbit

Purification Method

Affinity Chromatography

Regulatory Status

RUO

Gene ID (Entrez)

16907, 299625, 84823

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

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Description

  • Immunogen sequence: YILRAGQMVT VWAAGAGVAH SPPSTLVWKG QSSWGTGESF RTVLVNADGE EVAMRTVKKS SVMRENENGE EEEEEAEFGE EDLFHQQGDP RTTSRGCYVM Nuclear lamins form a network of intermediate-type filaments at the nucleoplasmic site of the nuclear membrane
  • Two main subtypes of nuclear lamins can be distinguished, i.e
  • A-type lamins and B-type lamins
  • The A-type lamins comprise a set of three proteins arising from the same gene by alternative splicing, i.e
  • lamin A, lamin C and lamin Adel 10, while the B-type lamins include two proteins arising from two distinct genes, i.e
  • lamin B1 and lamin B2
  • Recent evidence has revealed that mutations in A-type lamins give rise to a range of rare but dominant genetic disorders, including Emery-Dreifuss muscular dystrophy, dilated cardiomyopathy with conduction-system disease and Dunnigan-type familial partial lipodystrophy
  • In addition, the expression of A-type lamins coincides with cell differentiation and as A-type lamins specifically interact with chromatin, a role in the regulation of differential gene expression has been suggested for A-type lamins.