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EXPH5 Rabbit pAb (bs-2834R)  
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產品編號 bs-2834R
英文名稱 EXPH5 Rabbit pAb
中文名稱 EXPH5蛋白抗體
別    名 DKFZp586F1223; DKFZp781H0795; Exophilin 5; Exophilin5; KIAA0624; MGC133291; EXPH5_HUMAN; MGC134967; SLAC2-B; SLAC2B; slp homolog lacking C2 domains b; synaptotagmin-like homologue lacking C2 domains b; synaptotagmin-like protein homolog lacking C2 domains b.  
研究領域 細胞生物  信號轉導  G蛋白信號  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 (predicted: Human,Mouse,Rat,Rabbit)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 222 kDa
檢測分子量
細胞定位 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human EXPH5: 1-100/1989 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 May act as Rab effector protein and play a role in vesicle trafficking.

Function:
May act as Rab effector protein and play a role in vesicle trafficking.

Subunit:
Interacts with RAB27A (By similarity).

Tissue Specificity:
Expressed in keratinocytes.

DISEASE:
Epidermolysis bullosa, non-specific, autosomal recessive (EBNS) [MIM:615028]: A skin disease characterized by blistering of skin and mucosae, following minimal pressure or trauma. Various clinical types with different severity are recognized, ranging from severe mutilating forms to mild forms with limited and localized scarring, and less frequent extracutaneous manifestations. EBNS clinical features mainly comprise trauma-induced scale crusts and intermittent skin blistering. Some of the crusted areas are hemorrhagic and accompanied by occasional bruising. Most lesions clear over several weeks to leave slightly atrophic scars and moderate post-inflammatory hyperpigmentation. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Contains 1 RabBD (Rab-binding) domain.

SWISS:
Q9C0E2

Gene ID:
23086

Database links:

Entrez Gene: 23086 Human

Omim: 612878 Human

SwissProt: Q9C0E2 Human



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