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SNAP29 Rabbit pAb (bs-11363R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-11363R
英文名称 SNAP29 Rabbit pAb
中文名称 突触相关蛋白29抗体
别    名 CEDNIK; SNAP-29; 1300018G05Rik; Gs32; SNP29_HUMAN; SNAP29; Soluble 29 kDa NSF attachment protein; Vesicle-membrane fusion protein SNAP-29; SNP29_MOUSE; Golgi SNARE of 32 kDa (Gs32); SNP29_RAT;   
研究领域 细胞生物  神经生物学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 Mouse (predicted: Human,Rat,Rabbit,Horse)
产品应用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 29 kDa
检测分子量 29
细胞定位 细胞浆 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SNAP29: 181-258/258 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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.

Function:
SNAREs, Soluble N-ethylmaleimide-sensitive factor-attachment protein receptors, are essential proteins for fusion of cellular membranes. SNAREs localized on opposing membranes assemble to form a trans-SNARE complex, an extended, parallel four alpha-helical bundle that drives membrane fusion. SNAP29 is a SNARE involved in autophagy through the direct control of autophagosome membrane fusion with the lysososome membrane. Probably involved in multiple membrane trafficking steps.

Subunit:
Interacts with multiple syntaxins including STX6 (By similarity). Forms a SNARE complex, composed of VAMP8, SNAP29 and STX17, involved in fusion of autophagosome with lysosome.

Subcellular Location:
Cytoplasm. Membrane; Peripheral membrane protein. Cell junction, synapse, synaptosome. Note=Appears to be mostly membrane-bound, probably via interaction with syntaxins, but a significant portion is cytoplasmic.

Tissue Specificity:
Found in brain, heart, kidney, liver, lung, placenta, skeletal muscle, spleen and pancreas.

DISEASE:
Defects in SNAP29 are the cause of CEDNIK syndrome (CEDNIK) [MIM:609528]. CEDNIK is a neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma

Similarity:
Belongs to the SNAP-25 family.
Contains 1 t-SNARE coiled-coil homology domain.

SWISS:
O95721

Gene ID:
9342

Database links:

Entrez Gene: 9342 Human

Entrez Gene: 67474 Mouse

Entrez Gene: 116500 Rat

Omim: 604202 Human

SwissProt: O95721 Human

SwissProt: Q9ERB0 Mouse

SwissProt: Q9Z2P6 Rat



产品图片
Sample: Lung (Mouse) Lysate at 40 ug Primary: Anti- SNAP29 (bs-11363R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 29 kD Observed band size: 29 kD
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