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PIPA584362

PEX3 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA584362-Each-of-1 In Stock ₹ 53,400.00

PIPA584362 - Each of 1

₹ 53,400.00

In Stock

Quantity

1

Base Price: ₹ 53,400.00

GST (18%): ₹ 9,612.00

Total Price: ₹ 63,012.00

Antigen

PEX3

Classification

Polyclonal

Conjugate

Unconjugated

Gene

PEX3

Gene Alias

1700014F15Rik; 2810027F19Rik; 2900010N04Rik; PBD10A; Peroxin3; peroxin-3; peroxisomal assembly protein 3; peroxisomal assembly protein PEX3; Peroxisomal biogenesis factor 3; pex3; transformation-related protein 18; TRG18; zgc:56313

Host Species

Rabbit

Purification Method

Anitgen affinity chromatography, Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

8504

Content And Storage

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

Form

Liquid

Applications

Immunohistochemistry, Western Blot

Concentration

0.2 mg/mL

Formulation

PBS with 40% glycerol and 0.02% sodium azide; pH 7.2

Gene Accession No.

P56589

Gene Symbols

PEX3

Immunogen

Recombinant protein corresponding to Human PEX3

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Description

  • Immunogen sequence: SLLDLEQKLK EIRNLVEQHK SSSWINKDGS KPLLCHYMMP DEETPLAVQA CGLSPRDITT IKLLNETRDM LESPDFSTVL N Peroxin 3, also known as PEX3 (peroxisomal biogenesis factor 3) or TRG18, is a 373 amino acid multi-pass membrane protein that localizes to peroxisomes and belongs to the Peroxin family
  • Expressed ubiquitously, Peroxin 3 interacts with Peroxin 19 and is involved in peroxisome biosynthesis and membrane vesicle assembly, as well as in the maintenance of peroxisomal integrity
  • Additionally, Peroxin 3 acts as a docking factor for Peroxin 19 and is required for the import of peroxisomal proteins
  • Defects in the gene encoding Peroxin 3 are the cause of peroxisome biogenesis disorder complementation group 12 (PBD-CG12) and Zellweger syndrome (ZwS), both of which arise from a failure of peroxisomal protein import.