ABCD2 Polyclonal Antibody

Elabscience
Product Code: E-AB-66659
Product Group: Primary Antibodies
Supplier: Elabscience
CodeSizePrice
E-AB-66659-60uL60uL£210.00
Quantity:
E-AB-66659-120uL120uL£291.00
Quantity:
E-AB-66659-200uL200uL£431.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
  • Human
  • Mouse
  • Rat
Application: Immunofluorescence (IF)
Shipping:
Ice packs
Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Images

1 / 2
Immunofluorescence analysis of L929 cells using ABCD2 Polyclonal Antibody at dilution of  1:100 (40x lens). Blue: DAPI for nuclear staining.
2 / 2
Immunofluorescence analysis of U-2 OS cells using ABCD2 Polyclonal Antibody at dilution of  1:100 (40x lens). Blue: DAPI for nuclear staining.

Immunofluorescence analysis of L929 cells using ABCD2 Polyclonal Antibody at dilution of  1:100 (40x lens). Blue: DAPI for nuclear staining.
Immunofluorescence analysis of U-2 OS cells using ABCD2 Polyclonal Antibody at dilution of  1:100 (40x lens). Blue: DAPI for nuclear staining.

Documents

Further Information

Abbreviation:
ABCD2
Background:
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. The function of this peroxisomal membrane protein is unknown; however this protein is speculated to function as a dimerization partner of ABCD1 and/or other peroxisomal ABC transporters. Mutations in this gene have been observed in patients with adrenoleukodystrophy, a severe demyelinating disease. This gene has been identified as a candidate for a modifier gene, accounting for the extreme variation among adrenoleukodystrophy phenotypes. This gene is also a candidate for a complement group of Zellweger syndrome, a genetically heterogeneous disorder of peroxisomal biogenesis.
Buffer:
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Concentration:
1mg/mL
Conjugation:
Unconjugated
Dilution:
IF 1:50-1:100
Immunogen:
Recombinant fusion protein of human ABCD2 (NP_005155.1).
Purification method:
Affinity purification
Target Synonym:
ABCD2;ABC39;ALDL1;ALDR;ALDRP;hALDR
UNIProt ID:
Q9UBJ2