ACAD9 Antibody (PACO15249)
- SKU:
- PACO15249
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- IHC
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
抗体名: | ACAD9 Antibody (PACO15249) |
抗体コード: | PACO15249 |
サイズ: | 50ul |
宿主種: | Rabbit |
申し込み: | ELISA, IHC |
推奨される希釈: | ELISA:1:2000-1:5000, IHC:1:25-1:100 |
反応性: | Human, Mouse |
免疫原: | Fusion protein of human ACAD9 |
憲法: | Liquid |
ストレージバッファ: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
精製方法: | Antigen affinity purification |
抗体のクローン性: | Polyclonal |
アイソタイプ: | IgG |
Conjugate: | Non-conjugated |
The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using PACO15249(ACAD9 Antibody) at dilution 1/10, on the right is treated with fusion protein. (Original magnification: x200). | |
The image on the left is immunohistochemistry of paraffin-embedded Human cervical cancer tissue using PACO15249(ACAD9 Antibody) at dilution 1/10, on the right is treated with fusion protein. (Original magnification: x200). |
バックグラウンド: | This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants. |
シノニム: | acyl-CoA dehydrogenase family, member 9 |
UniProt Protein Function: | ACAD9: Has a dehydrogenase activity on palmitoyl-CoA (C16:0) and stearoyl-CoA (C18:0). It is three times more active on palmitoyl-CoA then on stearoyl-CoA. Has little activity on octanoyl-CoA (C8:0), butyryl-CoA (C4:0) or isovaleryl-CoA (5:0). Belongs to the acyl-CoA dehydrogenase family. |
UniProt Protein Details: | Protein type:EC 1.3.99.-; Mitochondrial; Oxidoreductase Chromosomal Location of Human Ortholog: 3q21.3 Cellular Component: dendrite; mitochondrial inner membrane; mitochondrion; nucleus Molecular Function:acyl-CoA binding; acyl-CoA dehydrogenase activity; electron carrier activity; FAD binding; protein binding Biological Process: fatty acid beta-oxidation using acyl-CoA dehydrogenase; lipid homeostasis; mitochondrial respiratory chain complex I assembly Disease: Acyl-coa Dehydrogenase Family, Member 9, Deficiency Of |
NCBI Summary: | This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010] |
UniProt Code: | Q9H845 |
NCBI GenInfo Identifier: | 21361497 |
NCBI Gene ID: | 28976 |
NCBI Accession: | |
UniProt Secondary Accession: | Q9H845,Q8WXX3, D3DNB8, |
UniProt Related Accession: | Q9H845 |
Molecular Weight: | 69kDa |
NCBI Full Name: | acyl-CoA dehydrogenase family member 9, mitochondrial |
NCBI Synonym Full Names: | acyl-CoA dehydrogenase family member 9 |
NCBI Official Symbol: | ACAD9 |
NCBI Official Synonym Symbols: | NPD002 |
NCBI Protein Information: | acyl-CoA dehydrogenase family member 9, mitochondrial |
UniProt Protein Name: | Acyl-CoA dehydrogenase family member 9, mitochondrial |
Protein Family: | Acyl-CoA dehydrogenase family |
UniProt Gene Name: | ACAD9 |
UniProt Entry Name: | ACAD9_HUMAN |
Antibodies |
Anti-ACAD9 Antibody (CAB14121) |
Anti-ACAD9 Antibody (CAB7798) |
Anti-ACAD9 Antibody (CAB19942)[KO Validated] |
ACAD9 Antibody (PACO03971) |
ACAD9 Antibody (PACO07543) |
Secondary Antibody |
Anti-HRP Goat Anti-Rabbit IgG (H+L) Antibody (CABS014) |
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