ABCD1 Mouse Monoclonal Antibody [Clone ID: OTI4C2]
CAT#: TA803208
ABCD1 mouse monoclonal antibody, clone OTI4C2 (formerly 4C2)
Size: 30 ul
Formulation: Carrier-Free
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Specifications
Product Data | |
Clone Name | OTI4C2 |
Applications | IHC, WB |
Recommend Dilution | WB 1:2000, IHC 1:150 |
Reactivity | Human |
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 | PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide. |
Concentration | 1 mg/ml |
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 |
Citations (7)
The use of this Antibodies has been cited in the following citations: |
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In vivo gene editing via homology-independent targeted integration for adrenoleukodystrophy treatment
,Hong, SA;Seo, JH;Wi, S;Jung, ES;Yu, J;Hwang, GH;Yu, JH;Baek, A;Park, S;Bae, S;Cho, SR;,
Molecular therapy : the journal of the American Society of Gene Therapy
,PubMed ID 34058389
[ABCD1]
|
Generation of a WA14 hESC sub-line carrying a hemizygous ABCD1 (C.1696_1710 del) mutation introduced by CRISPR/Cas9 technology
,Hong, W;Yun, W;Choi, W;Son, D;Song, G;You, S;,
Stem cell research
,PubMed ID 33611043
[ABCD1]
|
Successful Correction of ALD Patient-derived iPSCs Using CRISPR/Cas9
,Jung, ES;Quan, Z;Chang, MY;Kim, JH;Kim, SH;You, S;,
bioRxiv
[ABCD1]
|
SIRT1 activation alleviates brain microvascular endothelial dysfunction in peroxisomal disorders
,Zhang, Y;Cui, G;Wang, Y;Gong, Y;Wang, Y;,
Int. J. Mol. Med.
,PubMed ID 31257461
[ABCD1]
|
Intrathecal Adeno-Associated Virus Vector-mediated Gene Delivery for Adrenomyeloneuropathy
,Gong, Y;Berenson, A;Laheji, F;Gao, G;Wang, D;Ng, C;Volak, A;Kok, R;Kreouzis, V;Dijkstra, I;Kemp, S;Maguire, CA;Eichler, F;,
Hum. Gene Ther.
,PubMed ID 30358470
[ABCD1]
|
Microglial dysfunction as a key pathologic change in adrenomyeloneuropathy
,Gong, Y;Sasidharan, N;Laheji, F;Frosch, M;Musolino, P;Tanzi, R;Kim, DY;Biffi, A;El Khoury, J;Eichler, F;,
Ann. Neurol.
,PubMed ID 29059709
[ABCD1]
|
Brain endothelial dysfunction in cerebral adrenoleukodystrophy
,Musolino, PL;Gong, Y;Snyder, JM;Jimenez, S;Lok, J;Lo, EH;Moser, AB;Grabowski, EF;Frosch, MP;Eichler, FS;,
Brain
,PubMed ID 26377633
[ABCD1]
|
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抗体相关资料 |
Other Versions
SKU | Description | Size | Price |
---|---|---|---|
CF803208 | Carrier-free (BSA/glycerol-free) ABCD1 mouse monoclonal antibody, clone OTI4C2 (formerly 4C2) |
CNY 3,999.00 |
|
TA803208AM | ABCD1 mouse monoclonal antibody,clone 4C2, Biotinylated |
CNY 3,990.00 |
|
TA803208BM | ABCD1 mouse monoclonal antibody,clone 4C2, HRP conjugated |
CNY 3,990.00 |
|
TA803208S | ABCD1 mouse monoclonal antibody, clone OTI4C2 (formerly 4C2) |
CNY 800.00 |