ALX4 抗体 (AA 1-220)
Quick Overview for ALX4 抗体 (AA 1-220) (ABIN1678646)
抗原
See all ALX4 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1-220
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序列
- MNAETCVSYC ESPAAAMDAY YSPVSQSREG SSPFRAFPGG DKFGTTFLSA AAKAQGFGDA KSRARYGAGQ QDLATPLESG AGARGSFNKF QPQPSTPQPQ PPPQPQPQQQ QPQPQPPAQP HLYLQRGACK TPPDGSLKLQ EGSSGHSAAL QVPCYAKESS LGEPELPPDS DTVGMDSSYL SVKEAGVKGP QDRASSDLPS PLEKADSESN KGKKRRNRTT
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交叉反应
- 人, 小鼠, 大鼠
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产品特性
- Polyclonal Antibodies
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-220 of human ALX4 (NP_068745.2).
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亚型
- IgG
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anti-ALX Homeobox 4 (ALX4) (AA 249-275) antibody
ALX4 适用: 人 WB, FACS, CUT&RUN 宿主: 兔 Polyclonal RB28072 unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人 WB, IHC, IF, IHC (p) 宿主: 小鼠 Monoclonal 6B3 unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 2F2 unconjugated
anti-ALX Homeobox 4 (ALX4) (AA 112-216) antibodyALX4 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) antibodyALX4 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (AA 31-80) antibodyALX4 适用: 人, 小鼠, 犬, Cow, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (AA 151-200) antibodyALX4 适用: 人, 小鼠, 大鼠, 犬, Cow, 豚鼠, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (C-Term) antibodyALX4 适用: 人, 犬, Cow, 兔, 马, 豚鼠, 猴, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-ALX Homeobox 4 (ALX4) (N-Term) antibodyALX4 适用: 人, 大鼠, 犬, 马, 猴, Drosophila melanogaster WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB,1:500 - 1:2000,IHC,1:50 - 1:200
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限制
- 仅限研究用
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缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- ALX4 (ALX Homeobox 4 (ALX4))
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别名
- ALX4
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背景
- This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2), an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism, suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS), a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart.,ALX4,CRS5,FND2,Epigenetics & Nuclear Signaling,Transcription Factors,ALX4
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分子量
- 44 kDa
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基因ID
- 60529
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UniProt
- Q9H161
抗原
-
