SLC26A6 Knockout NCI-H1299 Cell Pool

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LM01019225697

Product ID: LM01019225697

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隐藏域元素占位

  • 产品描述
  • 细胞复苏
  • 细胞传代
  • 细胞冻存
  • 抗体验证结果
    • Brand: ELEM粒曼
    • Commodity name: SLC26A6 Knockout NCI-H1299 Cell Pool
    • Commodity ID: LM01019225697
    • Gene Symbol: SLC26A6
    • Ensembl ID: ENSG00000225697
    • Uniprot ID: Q9BXS9
    • 宿主细胞 / 类型: NCI-H1299/人非小细胞肺癌细胞
    • NCBI Gene ID: 65010
    • 规格: 1×10^6 cells/ 冻存管
    • 生长培养基: RPMI-1640+10%FBS+1%P/S
    • 筛选标记: N/A
    • 生长特性: 贴壁细胞,上皮细胞样
    • 培养条件: 37℃,5% CO2 的培养箱,1/3到 1/4 传代
    • 倍增时间: ~24-48 h
    • 参考换液频率: 2~3次/周
    • 支原体检测结果: 阴性
    • 敲除效率(Sanger测序): >70%
    • 蛋白质组验证结果: N/A
    • 抗体货号: 添加中
    • 目标基因介绍: [Isoform 4]: Apical membrane chloride-bicarbonate exchanger. Its association with carbonic anhydrase CA2 forms a bicarbonate transport metabolon; hence maximizes the local concentration of bicarbonate at the transporter site.||Apical membrane anion-exchanger with wide epithelial distribution that plays a role as a component of the pH buffering system for maintaining acid-base homeostasis. Acts as a versatile DIDS-sensitive inorganic and organic anion transporter that mediates the uptake of monovalent anions like chloride, bicarbonate, formate and hydroxyl ion and divalent anions like sulfate and oxalate. Functions in multiple exchange modes involving pairs of these anions, which include chloride-bicarbonate, chloride-oxalate, oxalate-formate, oxalate-sulfate and chloride-formate exchange. Apical membrane chloride-bicarbonate exchanger that mediates luminal chloride absorption and bicarbonate secretion by the small intestinal brush border membrane and contributes to intracellular pH regulation in the duodenal upper villous epithelium during proton-coupled peptide absorption, possibly by providing a bicarbonate import pathway. Mediates also intestinal chloride absorption and oxalate secretion, thereby preventing hyperoxaluria and calcium oxalate urolithiasis. Transepithelial oxalate secretion, chloride-formate, chloride-oxalate and chloride-bicarbonate transport activities in the duodenum are inhibited by PKC activation in a calcium-independent manner. The apical membrane chloride-bicarbonate exchanger provides also a major route for fluid and bicarbonate secretion into the proximal tubules of the kidney as well as into the proximal part of the interlobular pancreatic ductal tree, where it mediates electrogenic chloride-bicarbonate exchange with a chloride-bicarbonate stoichiometry of 1:2, and hence will dilute and alkalinize protein-rich acinar secretion. Mediates also the transcellular sulfate absorption and oxalate secretion across the apical membrane in the duodenum and the formate ion efflux at the apical brush border of cells in the proximal tubules of kidney. Plays a role in sperm capacitation by increasing intracellular pH.
    • 细胞开发路径: 采用CRISPR-RNP方法生成稳定KO Cell Pool;Sanger 测序结果显示KO Cell Pool敲除效率>70%。
    • 应用: 高敲除效率的基因敲除细胞池(KO Cell Pool),特别适用于初步功能分析、复杂疾病模型的开发、精准药物筛选以及广泛的基因发现研究。KO pool能够无需繁琐的单克隆挑选过程,直接应用于多种类型的测定和分析,大幅提升实验效率。
    Key words:
    • SLC26A6
  • 01.  在 37℃水浴中预热完全培养基。
    02.  将冻存管在 37℃水浴中解冻 1-2 分钟。
    03.  将冻存管转移到生物安全柜中,并用 70% 乙醇擦拭表面。
    04.  拧开冻存管管盖,将细胞悬液轻轻转移到含有 9mL 完全培养基的无菌离心管中。
    05.  在室温下以 125g 离心 5-7 分钟,弃上清。
    06.  用 5mL 的完整培养基重悬细胞沉淀,将细胞悬液转移到 T25 培养瓶中。
    07.  将细胞转移到 37℃,5% CO2 的培养箱中培养。
    08.  参考传代比例:1/3到 1/4 传代,2-3 天长满。

  • 01.  待培养瓶中细胞汇合度至 80%-90% 以上,可进行细胞传代。
    02.  将培养基、PBS、胰酶(0.25%Trypsin_EDTA Gibco 25200-056) 等从 4℃冰箱中拿出, 置于 37℃水浴中温度接近 37℃时取出并在瓶子表面喷洒 75% 酒精后置于生物安全柜中。

    03.  从培养箱中取出待传代的培养瓶,瓶身喷洒 75% 酒精后置于生物安全柜中。
    04.  为避免冲散细胞,沿培养瓶上壁 PBS 润洗细胞,清洗细胞后弃去,T25 加 2mL。
    05.  加入对应体积的胰酶(T75 加 1.5mL, T25 加 0.5mL)  ,并轻轻晃动瓶身使胰酶平铺满细胞 底部。可根据实际情况适当增加或减少用量。约 1-2min 后大部分细胞脱落时,加入对应体积的完全培养基终止消化,并用 5mL 移液管轻轻吹打至细胞全部脱落。
    06.  将细胞悬液转移至 15mL 离心管,悬液 300g 离心 5min,弃上清。
    07.  移取 5mL 完全培养基重悬细胞,按需求调整接种比例,并补充培养瓶中完全培养基,T75 加至 13-15mL,T25 加至 5mL,加 1% 双抗。
    08.  盖上瓶盖拧紧后轻轻晃动瓶身,使细胞混合均匀后置于 37℃,5% CO2 培养箱中。

  • 01.  准备冻存液,并提前预冷。
    02.  确保待冻存的细胞满足冻存要求,用显微镜检查以下状态:健康的外观及形态特征、所处生 长周期(对数晚期)、无污染或衰退迹象。
    03.  对细胞进行消化及离心处理(具体步骤参考传代培养流程)
    04.  按照每管 1mL 的量添加冻存液重悬细胞,吹打均匀后分装至冻存管。
    05.  将细胞放在程序降温盒中,在 -80℃冰箱中冷冻。
    06.  后续将细胞转移到液氮罐中,以便长期储存。

  • 抗体验证中

Classification: Gene Knockout Cell Pool(KO Pool)

Cell Line Information

Gene Symbol

SLC26A6

NCBI Gene ID

65010

Ensembl ID

ENSG00000225697

Uniprot ID

Q9BXS9

Screening marker

N/A

Host cell/type

NCI-H1299/人非小细胞肺癌细胞

Specifications

1×10^6 cells/ 冻存管

Growth Medium

RPMI-1640+10%FBS+1%P/S

growth characteristics

贴壁细胞,上皮细胞样

culture condition

37℃,5% CO2 的培养箱,1/3到 1/4 传代

doubling time

~24-48 h

Reference fluid change frequency

2~3次/周

Mycoplasma test results

阴性

Knock-out validation

Knockout efficiency (Sanger sequencing)

>70%

Proteome Validation Results

N/A

Antibody number

添加中

Antibody validation results

抗体验证中

Cell Line Description

Introduction of target gene

[Isoform 4]: Apical membrane chloride-bicarbonate exchanger. Its association with carbonic anhydrase CA2 forms a bicarbonate transport metabolon; hence maximizes the local concentration of bicarbonate at the transporter site.||Apical membrane anion-exchanger with wide epithelial distribution that plays a role as a component of the pH buffering system for maintaining acid-base homeostasis. Acts as a versatile DIDS-sensitive inorganic and organic anion transporter that mediates the uptake of monovalent anions like chloride, bicarbonate, formate and hydroxyl ion and divalent anions like sulfate and oxalate. Functions in multiple exchange modes involving pairs of these anions, which include chloride-bicarbonate, chloride-oxalate, oxalate-formate, oxalate-sulfate and chloride-formate exchange. Apical membrane chloride-bicarbonate exchanger that mediates luminal chloride absorption and bicarbonate secretion by the small intestinal brush border membrane and contributes to intracellular pH regulation in the duodenal upper villous epithelium during proton-coupled peptide absorption, possibly by providing a bicarbonate import pathway. Mediates also intestinal chloride absorption and oxalate secretion, thereby preventing hyperoxaluria and calcium oxalate urolithiasis. Transepithelial oxalate secretion, chloride-formate, chloride-oxalate and chloride-bicarbonate transport activities in the duodenum are inhibited by PKC activation in a calcium-independent manner. The apical membrane chloride-bicarbonate exchanger provides also a major route for fluid and bicarbonate secretion into the proximal tubules of the kidney as well as into the proximal part of the interlobular pancreatic ductal tree, where it mediates electrogenic chloride-bicarbonate exchange with a chloride-bicarbonate stoichiometry of 1:2, and hence will dilute and alkalinize protein-rich acinar secretion. Mediates also the transcellular sulfate absorption and oxalate secretion across the apical membrane in the duodenum and the formate ion efflux at the apical brush border of cells in the proximal tubules of kidney. Plays a role in sperm capacitation by increasing intracellular pH.

Cell development path

采用CRISPR-RNP方法生成稳定KO Cell Pool;Sanger 测序结果显示KO Cell Pool敲除效率>70%。

Application

高敲除效率的基因敲除细胞池(KO Cell Pool),特别适用于初步功能分析、复杂疾病模型的开发、精准药物筛选以及广泛的基因发现研究。KO pool能够无需繁琐的单克隆挑选过程,直接应用于多种类型的测定和分析,大幅提升实验效率。

Cell Culture Instructions

Cell Resuscitation

01.  在 37℃水浴中预热完全培养基。
02.  将冻存管在 37℃水浴中解冻 1-2 分钟。
03.  将冻存管转移到生物安全柜中,并用 70% 乙醇擦拭表面。
04.  拧开冻存管管盖,将细胞悬液轻轻转移到含有 9mL 完全培养基的无菌离心管中。
05.  在室温下以 125g 离心 5-7 分钟,弃上清。
06.  用 5mL 的完整培养基重悬细胞沉淀,将细胞悬液转移到 T25 培养瓶中。
07.  将细胞转移到 37℃,5% CO2 的培养箱中培养。
08.  参考传代比例:1/3到 1/4 传代,2-3 天长满。

cell passage

01.  待培养瓶中细胞汇合度至 80%-90% 以上,可进行细胞传代。
02.  将培养基、PBS、胰酶(0.25%Trypsin_EDTA Gibco 25200-056) 等从 4℃冰箱中拿出, 置于 37℃水浴中温度接近 37℃时取出并在瓶子表面喷洒 75% 酒精后置于生物安全柜中。

03.  从培养箱中取出待传代的培养瓶,瓶身喷洒 75% 酒精后置于生物安全柜中。
04.  为避免冲散细胞,沿培养瓶上壁 PBS 润洗细胞,清洗细胞后弃去,T25 加 2mL。
05.  加入对应体积的胰酶(T75 加 1.5mL, T25 加 0.5mL)  ,并轻轻晃动瓶身使胰酶平铺满细胞 底部。可根据实际情况适当增加或减少用量。约 1-2min 后大部分细胞脱落时,加入对应体积的完全培养基终止消化,并用 5mL 移液管轻轻吹打至细胞全部脱落。
06.  将细胞悬液转移至 15mL 离心管,悬液 300g 离心 5min,弃上清。
07.  移取 5mL 完全培养基重悬细胞,按需求调整接种比例,并补充培养瓶中完全培养基,T75 加至 13-15mL,T25 加至 5mL,加 1% 双抗。
08.  盖上瓶盖拧紧后轻轻晃动瓶身,使细胞混合均匀后置于 37℃,5% CO2 培养箱中。

cell cryopreservation

01.  准备冻存液,并提前预冷。
02.  确保待冻存的细胞满足冻存要求,用显微镜检查以下状态:健康的外观及形态特征、所处生 长周期(对数晚期)、无污染或衰退迹象。
03.  对细胞进行消化及离心处理(具体步骤参考传代培养流程)
04.  按照每管 1mL 的量添加冻存液重悬细胞,吹打均匀后分装至冻存管。
05.  将细胞放在程序降温盒中,在 -80℃冰箱中冷冻。
06.  后续将细胞转移到液氮罐中,以便长期储存。