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货号： bs-21252R-Gold 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-21252R-Gold
- 英文名称
- Anti-SLC30A2/Gold
- 中文名称
- 胶体金标记的溶质载体转运蛋白家族30成员2抗体
- 别 名
- SLC30A2; Solute carrier family 30 (Zinc Transporter) member 2; Solute carrier family 30 member 2; Zinc transporter 2; ZnT-2; ZNT2_HUMAN.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul（10nm 15nm 35nm）
- 研究领域
- 肿瘤 细胞生物 信号转导 转运蛋白
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human,
- 产品应用
- IEM=1:20-200 IGS=1:20-200 GICA=1:20-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 35kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 0.4mg/1ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human SLC30A2
- 亚 型
- IgG
- 纯化方法
- affinity purified by Protein A
- 储 存 液
- 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
- 保存条件
- Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
- 产品介绍
- background:
The protein encoded by this gene is a zinc transporter that acts as a homodimer. The encoded protein plays a role in secreting zinc into breast milk. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]
Subcellular Location:
Lysosome membrane and Vacuole membrane.
DISEASE:
The disease is caused by mutations affecting the gene represented in this entry.
Disease description:A disorder occurring in breast-fed infants as a consequence of low milk zinc concentration in their nursing mothers, which cannot be corrected by maternal zinc supplementation. A large amount of zinc, an essential trace mineral, is required for normal growth particularly in infants, and breast milk normally contains adequate zinc to meet the requirement for infants up to 4 to 6 months of age. Zinc deficiency can lead to dermatitis, alopecia, decreased growth, and impaired immune function. The disorder shows autosomal dominant inheritance with incomplete penetrance.
Similarity:
Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family.
SLC30A subfamily.
Database links:Entrez Gene: 7780Human
Omim: 609617Human
SwissProt: Q9BRI3Human
Unigene: 143545Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.