PMP70 antibody (C-Term)

Catalog No. ABIN3030056

The Rabbit Polyclonal anti-PMP70 antibody is suitable to detect PMP70 in samples from Human, Mouse and Rat. It has been validated for WB, IF and IHC (p).

Quick Overview for PMP70 antibody (C-Term) (ABIN3030056)

Target: PMP70 (ABCD3) (ATP-Binding Cassette, Sub-Family D (Ald), Member 3 (ABCD3))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PMP70 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-PMP70 Antibody

Binding Specificity: C-Term

Purpose: PMP70 Antibody / ABCD3

Sequence: EFKQITEDTV EFGS

Purification: Antigen affinity

Immunogen: An amino acid sequence from the C-terminus of human PMP70 (EFKQITEDTVEFGS) was used as the immunogen for this PMP70 antibody.

Isotype: IgG

Application Details

Application Notes: The stated application concentrations are suggested starting amounts. Titration of the PMP70 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the PMP70 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for PMP70

Target: PMP70 (ABCD3) (ATP-Binding Cassette, Sub-Family D (Ald), Member 3 (ABCD3))

Alternative Name: PMP70

Background: 70 kDa peroxisomal membrane protein (PMP70), also called ATP-binding cassette sub-family D member 3, is a protein that in humans is encoded by the ABCD3 gene. The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. The gene was assigned to human chromosome 1p21-p22 by in situ hybridization. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders.

UniProt: P28288

Pathways: Monocarboxylic Acid Catabolic Process