SNAP29 抗体 (AA 181-258) (Alexa Fluor 350)
-
- 抗原 See all SNAP29 抗体
- SNAP29 (Synaptosomal-Associated Protein, 29kDa (SNAP29))
-
抗原表位
- AA 181-258
-
适用
- 小鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This SNAP29 antibody is conjugated to Alexa Fluor 350
-
应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SNAP29
- 亚型
- IgG
- Top Product
- Discover our top product SNAP29 Primary Antibody
-
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (AA 1-258) antibody
SNAP29 适用: 人 WB, ELISA, IF 宿主: 小鼠 Monoclonal 3E4-E6 unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) antibodySNAP29 适用: 人, 小鼠, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (AA 1-258) antibodySNAP29 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (AA 1-258) antibodySNAP29 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (AA 1-258) antibodySNAP29 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (AA 1-258) antibodySNAP29 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1C10 unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) antibodySNAP29 适用: 人, 小鼠, 大鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (AA 141-190) antibodySNAP29 适用: 人, 大鼠, 犬, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (AA 110-159) antibodySNAP29 适用: 小鼠, 大鼠, 犬, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Synaptosomal-Associated Protein, 29kDa (SNAP29) (Middle Region) antibodySNAP29 适用: 人, 小鼠, 大鼠, 兔, 犬, 豚鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
-
- 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
-
- 抗原
- SNAP29 (Synaptosomal-Associated Protein, 29kDa (SNAP29))
- 别名
- SNAP29 (SNAP29 产品)
- 别名
- snap29 antibody, MGC52674 antibody, MGC75781 antibody, SNAP29 antibody, 1300018G05Rik antibody, AI891940 antibody, AU020222 antibody, BB131856 antibody, Gs32 antibody, CEDNIK antibody, SNAP-29 antibody, synaptosome associated protein 29kDa L homeolog antibody, synaptosome associated protein 29kDa antibody, synaptosome associated protein 29 antibody, synaptosomal-associated protein 29 antibody, snap29.L antibody, snap29 antibody, SNAP29 antibody, Snap29 antibody
- 背景
-
Synonyms: SNAP 29, SNAP-29, SNAP29, SNP29_HUMAN, Soluble 29 kDa NSF attachment protein, Synaptosomal associated protein 29, Synaptosomal associated protein 29 kDa, Synaptosomal-associated protein 29, Vesicle membrane fusion protein SNAP 29, Vesicle membrane fusion protein SNAP29, Vesicle-membrane fusion protein SNAP-29, CEDNIK, FLJ21051.
Background: SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
- 基因ID
- 9342
-
