ABCD1 Mouse Monoclonal Antibody [Clone ID: OTI2C12]
CAT#: CF803207
Carrier-free (BSA/glycerol-free) ABCD1 mouse monoclonal antibody, clone OTI2C12 (formerly 2C12)
Formulation: Standard
View other "OTI2C12" antibodies (4)
Need it in bulk or conjugated?
Get a free quote
CNY 3,999.00
Specifications
Product Data | |
Clone Name | OTI2C12 |
Applications | IHC, WB |
Recommend Dilution | WB 1:2000, IHC 1:150 |
Reactivity | Human, Mouse, Rat |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Human recombinant protein fragment corresponding to amino acids 508-745 of human ABCD1 (NP_000024) produced in E.coli. |
Formulation | Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) |
Reconstitution Method | For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) |
Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
Conjugation | Unconjugated |
Storage Condition | Store at -20°C as received. |
Predicted Protein Size | 82.8 kDa |
Gene Name | ATP binding cassette subfamily D member 1 |
Database Link | |
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. This peroxisomal membrane protein is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder of the nervous system. [provided by RefSeq, Jul 2008] |
Synonyms | ABC42; ALD; ALDP; AMN |
Reference Data | |
Protein Families | Druggable Genome |
Protein Pathways | ABC transporters |
Documents
Product Manuals |
FAQs |
SDS |
Resources
抗体相关资料 |
Other Versions
SKU | Description | Size | Price |
---|---|---|---|
TA803207 | ABCD1 mouse monoclonal antibody, clone OTI2C12 (formerly 2C12) |
CNY 1,999.00 |
|
TA803207AM | ABCD1 mouse monoclonal antibody,clone 2C12, Biotinylated |
CNY 3,990.00 |
|
TA803207BM | ABCD1 mouse monoclonal antibody,clone 2C12, HRP conjugated |
CNY 3,990.00 |
|
TA803207S | ABCD1 mouse monoclonal antibody, clone OTI2C12 (formerly 2C12) |
CNY 800.00 |