SCXA 抗体 (full length)
This 小鼠 单克隆 antibody specifically detects SCXA in FACS 和 IF. It exhibits reactivity toward 人.
产品编号 ABIN7878977
发货至:
中国
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Contact Info
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中国
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北京 101111
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Quick Overview for SCXA 抗体 (full length) (ABIN7878977)
抗原
See all SCXA 抗体
SCXA
(Scleraxis (SCXA))
适用
人
宿主
小鼠
克隆类型
单克隆
标记
This SCXA antibody is un-conjugated
应用范围
Flow Cytometry (FACS), Immunofluorescence (IF)
克隆位点
PCRP-SCXA-2D11
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抗原表位
- full length
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原理
- SCXA Antibody / Scleraxis
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纯化方法
- Protein A/G affinity
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免疫原
- Recombinant full-length human Basic helix-loop-helix transcription factor scleraxis protein was used as the immunogen for the SCXA antibody.
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亚型
- IgG2a
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anti-Scleraxis (SCXA) (AA 172-201), (C-Term) antibody
SCXA 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB30107 unconjugated
anti-Scleraxis (SCXA) (AA 165-200) antibodySCXA 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the SCXA antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.2 mg/mL
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缓冲液
- 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Aliquot the SCXA antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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- SCXA (Scleraxis (SCXA))
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别名
- SCXA
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背景
- Transcription factors are proteins that bind DNA adjacent to genes and control the production of mRNA transcripts. Scleraxis (basic helix-loop-helix transcription factor scleraxis) is a 201 amino acid protein that dimerizes with another bHLH protein to initiate transcription. Scleraxis is known to play a role in formation of mesoderm and somite-derived chondrogenic lineages. Scleraxis localizes to the nucleus and contains one bHLH domain. bHLH transcription factors, in general, function in cellular differentiation, proliferation, and oncogene regulation. The gene encoding Scleraxis maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
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UniProt
- Q7RTU7
抗原
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