SPATA5L1 抗体 (AA 221-320) (AbBy Fluor® 594)
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- 抗原 See all SPATA5L1 products
- SPATA5L1 (Spermatogenesis Associated 5-Like 1 (SPATA5L1))
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抗原表位
- AA 221-320
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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 SPATA5L1 antibody is conjugated to AbBy Fluor® 594
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SPATA5L1
- 亚型
- IgG
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anti-Spermatogenesis Associated 5-Like 1 (SPATA5L1) (AA 1-426) antibody
SPATA5L1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Spermatogenesis Associated 5-Like 1 (SPATA5L1) (AA 580-629) antibodySPATA5L1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- SPATA5L1 (Spermatogenesis Associated 5-Like 1 (SPATA5L1))
- 别名
- SPATA5L1 (SPATA5L1 产品)
- 别名
- spermatogenesis associated 5 like 1 antibody, SPATA5L1 antibody
- 背景
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Synonyms: FLJ12286, MGC5347, SPA5L_HUMAN, SPATA5L1, Spermatogenesis-associated protein 5-like protein 1.
Background: SPATA5L1 is a 753 amino acid protein belonging to the AAA ATPase family and AFG2 subfamily. Single nucleotide polymorphisms (SNPs) present in SPATA5L1 at the glycine amidinotransferase (GATM)-SPATA5L1 locus have been found to correlate with glomerular filtration rate (GFR), having significant implications for kidney disease research. SPATA5L1 localizes to cytoplasm and exists as three alternatively spliced isoforms. The gene encoding SPATA5L1 maps to human chromosome 15q21.1. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and comprises about 3 % of the human genome. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
- 基因ID
- 79029
- UniProt
- Q9BVQ7
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