C19orf28 抗体 (Alexa Fluor 750)
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- 抗原 See all C19orf28 products
- C19orf28 (Chromosome 19 Open Reading Frame 28 (C19orf28))
- 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 C19orf28 antibody is conjugated to Alexa Fluor 750
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应用范围
- Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human MFSD12/C19orf28
- 亚型
- IgG
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anti-Chromosome 19 Open Reading Frame 28 (C19orf28) (Middle Region) antibody
C19orf28 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 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
- C19orf28 (Chromosome 19 Open Reading Frame 28 (C19orf28))
- 别名
- C19orf28 (C19orf28 产品)
- 别名
- MGC81076 antibody, C19orf28 antibody, PP3501 antibody, F630110N24Rik antibody, Wdt1 antibody, major facilitator superfamily domain containing 12 L homeolog antibody, major facilitator superfamily domain containing 12 antibody, mfsd12.L antibody, mfsd12 antibody, MFSD12 antibody, Mfsd12 antibody
- 背景
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Synonyms: Chromosome 19 open reading frame 28, Hypothetical protein LOC126321, MGC20700, PP3501, Uncharacterized MFS type transporter C19orf28, MFS12_HUMAN.
Background: C19orf28, also known as PP3501, is a multi-pass membrane protein that belongs to the major facilitator superfamily. The gene encoding C19orf28 localizes to chromosome 19 and, due to alternative splicing events, C19orf28 exists as two isoforms. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf28 gene product has been provisionally designated C19orf28 pending further characterization.
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