ABCD2 Antibody - BSA Free

Western Blot: ABCD2 Antibody - BSA Free [NBP3-48249] - Mouse cerebellum tissue were subjected to SDS PAGE followed by western blot with (ABCD2 Antibody) at dilution of 1:300

Immunoprecipitation: ABCD2 Antibody - BSA Free [NBP3-48249] - IP Result of anti-ABCD2 (IP:, 4ug; Detection: 1:300) with A431 cells lysate 1200ug.

• Reactivity: Hu, Mu, Rt
• Applications: WB, ELISA, IP
• Clonality: Polyclonal
• Host: Rabbit
• Conjugate: Unconjugated
• Format: BSA Free

ABCD2 Antibody - BSA Free Summary

• Immunogen: ATP-binding cassette, sub-family D(ALD), member 2. (Uniprot# Q9UBJ2)
• Isotype: IgG
• Clonality: Polyclonal
• Host: Rabbit
• Gene: ABCD2
• Purity: Immunogen affinity purified

Applications/Dilutions

• Dilutions:
  • ELISA
  • Immunoprecipitation 1:200-1:1000
  • Western Blot 1:200-1:1000
• Theoretical MW: 80 kDa.
  Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

• Storage: Store at -20C. Avoid freeze-thaw cycles.
• Buffer: PBS, 50% Glycerol, pH (7.3)
• Preservative: 0.02% Sodium Azide
• Purity: Immunogen affinity purified

Alternate Names for ABCD2 Antibody - BSA Free

• Adrenoleukodystrophy-like 1
• Adrenoleukodystrophy-related protein
• ALD1
• ALDL1ATP-binding cassette sub-family D member 2
• ALDRhALDR
• ALDRPABC39
• ATP-binding cassette, sub-family D (ALD), member 2

Background

The protein encoded by the ABCD2 gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABCproteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into sevendistinct 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 peroxisomalABC transporters are half transporters which require a partner half transporter molecule to form a functionalhomodimeric or heterodimeric transporter. The function of this peroxisomal membrane protein is unknown; however thisprotein 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. Thisgene has been identified as a candidate for a modifier gene, accounting for the extreme variation amongadrenoleukodystrophy phenotypes. This gene is also a candidate for a complement group of Zellweger syndrome, agenetically heterogeneous disorder of peroxisomal biogenesis. (provided by RefSeq)

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: ABCD2