PLOD1 抗体 (AA 23-640)
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- 抗原 See all PLOD1 抗体
- PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))
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抗原表位
- AA 23-640
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This PLOD1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA
- 原理
- Anti-PLOD1 Antibody Picoband®
- 交叉反应 （详细）
- No cross reactivity with other proteins.
- 产品特性
- Anti-PLOD1 Antibody Picoband® (ABIN7600763). Tested in ELISA, WB applications. This antibody reacts with Human. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
- 纯化方法
- Immunogen affinity purified.
- 免疫原
- E.coli-derived human PLOD1 recombinant protein (Position: K23-A640).
- 亚型
- IgG
- Top Product
- Discover our top product PLOD1 Primary Antibody
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anti-Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) (AA 66-94), (N-Term) antibody
PLOD1 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB30211 unconjugated
anti-Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) (AA 636-727) antibodyPLOD1 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) (AA 73-102), (N-Term) antibodyPLOD1 适用: 人 WB, FACS, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) (AA 19-114) antibodyPLOD1 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) (AA 488-727) antibodyPLOD1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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Western blot, 0.25-0.5 μg/mL, Human
ELISA, 0.1-0.5 μg/mL, -
1. Al-Gazali, L. I., Bakalinova, D., Varady, E., Scorer, J., Nork, M. Further delineation of Nevo syndrome. J. Med. Genet. 34: 366-370, 1997. 2. Brinckmann, J., Acil, Y., Feshchenko, S., Katzer, E., Brenner, R., Kulozik, A., Kugler, S. Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C). Arch. Derm. Res. 290: 181-186, 1998. 3. Dembure, P. P., Janko, A. R., Priest, J. H., Elsas, L. J. Ascorbate regulation of collagen biosynthesis in Ehlers-Danlos syndrome, type VI. Metabolism 36: 687-691, 1987. - 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
- 浓度
- 500 μg/mL
- 缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
- 储存条件
- 4 °C,-20 °C
- 储存方法
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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- 抗原
- PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))
- 别名
- PLOD1 (PLOD1 产品)
- 背景
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Synonyms: 70 kDa ribosomal protein S6 kinase 1 antibody, KS6B1_HUMAN antibody, p70 alpha antibody, P70 beta 1 antibody, p70 ribosomal S6 kinase alpha antibody, p70 ribosomal S6 kinase beta 1 antibody, p70 S6 kinase alpha antibody, P70 S6 Kinase antibody, p70 S6 kinase alpha 1 antibody, p70 S6 kinase alpha 2 antibody, p70 S6K antibody, p70 S6K-alpha antibody, p70 S6KA antibody, p70(S6K) alpha antibody, p70(S6K)-alpha antibody, p70-alpha antibody, p70-S6K 1 antibody, p70-S6K antibody, P70S6K antibody, P70S6K1 antibody, p70S6Kb antibody, PS6K antibody, Ribosomal protein S6 kinase 70 kDa polypeptide 1 antibody, Ribosomal protein S6 kinase beta 1 antibody, Ribosomal protein S6 kinase beta-1 antibody, Ribosomal protein S6 kinase I antibody, RPS6KB1 antibody, S6K antibody, S6K-beta-1 antibody, S6K1 antibody, Serine/threonine kinase 14 alpha antibody, Serine/threonine-protein kinase 14A antibody, STK14A antibody
Tissue Specificity: Expressed in all tissues.
Background: Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity. Two transcript variants encoding different isoforms have been found for this gene.
- 分子量
- 84 kDa
- 基因ID
- 5351
- UniProt
- Q02809
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