PIPA529598

Filamin A alpha-2 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA529598-Each-of-1 In Stock ₹ 46,591.50

PIPA529598 - Each of 1

₹ 46,591.50

In Stock

Quantity

1

Base Price: ₹ 46,591.50

GST (18%): ₹ 8,386.47

Total Price: ₹ 54,977.97

Antigen

Filamin A alpha-2

Classification

Polyclonal

Conjugate

Unconjugated

Gene

FLNA

Gene Alias

ABP-280; ABPX; actin binding protein 280; actin-binding protein 280; alpha filamin; alpha-filamin; CSBS; CVD1; dilated pupils 2; Dilp2; Endothelial actin-binding protein; Endothelial actin-binding protein 280); F730004A14Rik; filamin A; filamin A, alpha; filamin, alpha; filamin-1; Filamin-A; FLN; FLN1; FLNA; FLN-A; FMD; GENA 379; MNS; NHBP; Non-muscle filamin; OPD; OPD1; OPD2; RGD1560614; XLVD; XMVD

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

192176, 2316, 293860

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

0.42 mg/mL

Formulation

0.1M tris glycine with 20% glycerol and 0.01% thimerosal; pH 7

Gene Accession No.

P21333, Q8BTM8

Gene Symbols

FLNA

Immunogen

Recombinant fragment corresponding to a region within amino acids 1769 and 2098 of Human Filamin A alpha 2

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Recommended positive controls: 293T, A431, H1299, HeLa, HepG2, Molt-4, Raji, mouse kidney, PC-12, Rat2
  • Predicted reactivity: Mouse (98%), Rat (98%), Rabbit (98%), Bovine (99%)
  • Store product as a concentrated solution
  • Centrifuge briefly prior to opening the vial
  • The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins
  • The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration
  • This protein interacts with integrins, transmembrane receptor complexes, and second messengers
  • Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX)
  • Two transcript variants encoding different isoforms have been found for this gene.