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DDHD1 Rabbit pAb (bs-14221R)  
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產品編號 bs-14221R
英文名稱 DDHD1 Rabbit pAb
中文名稱 磷脂酶DDHD1抗體
別    名 DDHD domain containing 1; DDHD domain containing protein 1; KIAA1705; PA-PLA1; PAPLA1; Phosphatidic acid-preferring phospholipase A1 homolog; phospholipase DDHD1; Spastic paraplegia 28(autosomal recessive); SPG28.  
研究領域 細胞生物  信號轉導  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Dog)
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 100 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 DDHD1: 751-850/900 
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 Phosphatidic acid is released following cell activation and functions as a second messenger in several signaling pathways. DDHD1 is a lipase that catalyzes degradation of phosphatidic acid and attenuates cell activation.

Function:
Phospholipase that hydrolyzes phosphatidic acid, including 1,2-dioleoyl-sn-phosphatidic acid. The different isoforms may change the substrate specificity.

Subunit:
Forms homooligomers and, to a much smaller extent, heterooligomers with DDHD2.

Subcellular Location:
Cytoplasmic

Tissue Specificity:
Highly expressed in testis. Also expressed in brain, spleen and lung. Only expressed in cerebellum in fetal brain.

DISEASE:
Spastic paraplegia 28, autosomal recessive (SPG28) [MIM:609340]: A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. Some SPG28 patients also have distal sensory impairment. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the PA-PLA1 family.
Contains 1 DDHD domain.

SWISS:
Q8NEL9

Gene ID:
80821

Database links:

Entrez Gene: 80821 Human

Entrez Gene: 114874 Mouse

Entrez Gene: 305816 Rat

Omim: 614603 Human

SwissProt: Q8NEL9 Human

SwissProt: Q80YA3 Mouse

Unigene: 125525 Human

Unigene: 121918 Mouse

Unigene: 163271 Rat



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