HOXA2 Antibody, Biotin conjugated
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中文名稱：HOXA2兔多克隆抗體, Biotin偶聯
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貨號：CSB-PA010652LD01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) HOXA2 Polyclonal antibody
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Uniprot No.：
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基因名：HOXA2
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別名：AI324701 antibody; homeo box A2 antibody; homeobox A2 antibody; Homeobox protein Hox-1K antibody; Homeobox protein Hox-A2 antibody; Hox-1.11 antibody; HOX1.11 antibody; HOX1K antibody; Hoxa-2 antibody; Hoxa11 antibody; HOXA2 antibody; HXA2_HUMAN antibody; MGC151482 antibody; MGC151484 antibody; RATHOX111A antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human Homeobox protein Hox-A2 protein (26-124AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：Biotin
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：>95%, Protein G purified
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
產品提供形式：Liquid
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應用范圍：ELISA
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Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期：Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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功能：Sequence-specific transcription factor which is part of a developmental regulatory system that provides cells with specific positional identities on the anterior-posterior axis.
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基因功能參考文獻：
- Performed mutational analysis of TCOF1, GSC, and HOXA2 to determine the mutational features of the 3 genes in Chinese patients with Treacher Collins syndrome. PMID: 27526242
- The role of HOXA2 gene in dominant isolated microtia and the dysmorphogenetic effect of this gene on ear development PMID: 27503514
- 5 genomic variants in GSC, HOXA2 and PRKRA were identified through mutational analysis in Chinese patients with microtia. PMID: 28109504
- The Hoxa2-mediated decay of RCHY1 involves both the 19S and 20S proteasome complexes PMID: 26496426
- HOXA2 acts as a suppressor or TBP-antagonist to inhibit MMP-9 expression; while methylation-mediated inactivation of HOXA2 in NPC derepresses MMP-9 production and increases invasion of NPC cells. PMID: 24243817
- we have identified a nonsense mutation (Q235*) in HOXA2 that segregates with bilateral nonsyndromic microtia and hearing loss through three generations of a family in an autosomal dominant pattern. PMID: 23775976
- Lack of mutations in the coding region of HOXA2 among the sporadic microtia patients. PMID: 20542577
- A missense mutation in the HOXA2 in a consanguineous iranian family with bilateral microtia was reported. PMID: 18394579
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相關疾病：Microtia, hearing impairment, and cleft palate (MHICP); Microtia with or without hearing impairment (MCRT)
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亞細胞定位：Nucleus.
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蛋白家族：Antp homeobox family, Proboscipedia subfamily
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數據庫鏈接：
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