PEX10 antibody (Middle Region)

Catalog No. ABIN2781270

The Rabbit Polyclonal anti-PEX10 antibody has been validated for WB and IHC. It is suitable to detect PEX10 in samples from Human.

Quick Overview for PEX10 antibody (Middle Region) (ABIN2781270)

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PEX10 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Product Details anti-PEX10 Antibody

Binding Specificity: Middle Region

Sequence: QALRPDPLRV LMSVAPSALQ LRVRSLPGED LRARVSYRLL GVISLLHLVL

Predicted Reactivity: Human: 100%

Characteristics: This is a rabbit polyclonal antibody against PEX10. It was validated on Western Blot and immunohistochemistry.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the middle region of human PEX10

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 346 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for PEX10

Target: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Alternative Name: PEX10

Background: PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.
Alias Symbols: MGC1998, NALD, RNF69
Protein Interaction Partner: HNRNPD, PEX5, PEX14, LIG4, PCGF6, CGRRF1, MKRN3, PEX19, PEX12, PEX10, UBC, UBE2I, PEX2,
Protein Size: 346

Molecular Weight: 39 kDa

Gene ID: 5192

NCBI Accession: NM_153818, NP_722540

Pathways: Monocarboxylic Acid Catabolic Process