Gephyrin 抗体
Our Local Distributor
北京 101111
Quick Overview for Gephyrin 抗体 (ABIN2721817)
抗原
See all Gephyrin (GPHN) 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
-
-
产品特性
- Homo sapiens gephyrin (GPHN), transcript variant 1
-
纯化方法
- Purified from mouse ascites fluids by affinity chromatography
-
免疫原
- Full length human recombinant protein of human GPHN (NP_065857) produced in HEK293T cell.
-
亚型
- IgG2a
-
-
anti-Gephyrin (GPHN) antibody
GPHN 适用: 人, 猴 WB, IHC, FACS, IF, IHC (p) 宿主: 小鼠 Monoclonal 3B6 unconjugated
anti-Gephyrin (GPHN) (AA 148-736) antibodyGPHN 适用: 人, 小鼠, 大鼠, 猴 WB, IHC, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Gephyrin (GPHN) antibodyGPHN 适用: 人, 大鼠, 猴 WB, FACS 宿主: 小鼠 Monoclonal 3A6 unconjugated
anti-Gephyrin (GPHN) antibodyKD Validated GPHN 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 24GB5580 unconjugated
anti-Gephyrin (GPHN) antibodyKD Validated GPHN 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 24GB5585 unconjugated
anti-Gephyrin (GPHN) (AA 437-466) antibodyGPHN 适用: 人, 小鼠 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB24625 unconjugated
anti-Gephyrin (GPHN) antibodyGPHN 适用: 人, 小鼠, 大鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Gephyrin (GPHN) (AA 677-769) antibodyGPHN 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Gephyrin (GPHN) (AA 360-460) antibodyGPHN 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Gephyrin (GPHN) (AA 520-769) antibodyGPHN 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- WB 1:2000, FLOW 1:100
-
说明
-
The concentration of the product may vary between diferrent lots.
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 0.5-1.0 mg/mL
-
缓冲液
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
-
储存液
- Sodium azide
-
注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
储存条件
- -20 °C
-
-
- Gephyrin (GPHN)
-
别名
- GPHN
-
背景
- This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described, however, the full-length nature of all transcript variants is not currently known.
-
分子量
- 83.3 kDa
-
基因ID
- 10243
-
NCBI登录号
- NM_020806
-
HGNC
- 10243
-
途径
- Synaptic Membrane, Skeletal Muscle Fiber Development
抗原
-
