FGD1 抗体 (AA 50-100)
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- 抗原 See all FGD1 抗体
- FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))
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抗原表位
- AA 50-100
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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 FGD1 antibody is un-conjugated
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应用范围
- Immunoprecipitation (IP)
- 原理
- Rabbit anti-FGD1 Antibody, Affinity Purified
- 纯化方法
- Affinity Purified
- 免疫原
- Between AA 50 and 100
- 亚型
- IgG
- Top Product
- Discover our top product FGD1 Primary Antibody
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anti-FYVE, RhoGEF and PH Domain Containing 1 (FGD1) (AA 700-800) antibody
FGD1 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-FYVE, RhoGEF and PH Domain Containing 1 (FGD1) (C-Term) antibodyFGD1 适用: 人, Cow, 犬, Pig, 大鼠, 小鼠, 兔, 马 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-FYVE, RhoGEF and PH Domain Containing 1 (FGD1) (N-Term) antibodyFGD1 适用: 人, Cow, 犬, Pig, 兔 WB 宿主: 兔 Polyclonal unconjugated
anti-FYVE, RhoGEF and PH Domain Containing 1 (FGD1) (C-Term) antibodyFGD1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-FYVE, RhoGEF and PH Domain Containing 1 (FGD1) (N-Term) antibodyFGD1 适用: 人, Cow, Pig, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-FYVE, RhoGEF and PH Domain Containing 1 (FGD1) antibodyFGD1 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IP: 2 - 10 μg/mg lysate
WB: Not recommended. ABIN7451132 has not performed satisfactorily when used for WB of FGD1 in crude preparations (e.g. whole cell lysate). This antibody can be used for WB of enriched (e.g. immunoprecipitated) sources of FGD1.
- 限制
- 仅限研究用
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- 浓度
- 1000 μg/mL
- 缓冲液
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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
- 4 °C
- 有效期
- 12 months
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- 抗原
- FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))
- 别名
- FGD1 (FGD1 产品)
- 别名
- AAS antibody, FGDY antibody, MRXS16 antibody, ZFYVE3 antibody, FYVE, RhoGEF and PH domain containing 1 antibody, FGD1 antibody, Fgd1 antibody, fgd1 antibody
- 背景
- Background: The gene FGD1 encodes for FYVE, RhoGEF and PH domain-containing protein 1. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs. Defects in this gene are the cause of faciogenital dysplasia and X-linked mental retardation, syndromatic 16 [taken from NCBI Entrez Gene (Gene ID: 2245)].
- 基因ID
- 2245
- UniProt
- P98174
- 途径
- Neurotrophin Signaling Pathway
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