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進口Cellabs卡氏肺孢子蟲免疫熒光檢測試劑

進口Cellabs卡氏肺孢子蟲免疫熒光檢測試劑

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Cellabs是一家擁有*生物技術的公司,其總部設在澳大利亞的悉尼。從事銷售、研發和生產熱帶傳染病免疫診斷試劑。進口Cellabs卡氏肺孢子蟲免疫熒光檢測試劑廣州健侖生物科技有限公司提供服務!

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進口Cellabs卡氏肺孢子蟲免疫熒光檢測試劑

廣州健侖生物科技有限公司

廣州健侖長期供應各種生物原料,主要代理品牌:美國Seracare、西班牙Certest、美國Fuller、美國NOVABIOS、 Cellabs等等。

Cellabs公司是一個的生物技術公司,總部位于澳大利亞悉尼。專門研發與生產針對熱帶傳染性疾病的免疫診斷試劑盒。其產品40多個國家和地區。1998年,Cellabs收購TropBio公司,進一步鞏固其在研制熱帶傳染病、寄生蟲診斷試劑方面的位置。

進口Cellabs卡氏肺孢子蟲免疫熒光檢測試劑
    該公司的Crypto/Giardia Cel IFA是國標*推薦的兩蟲檢測IFA染色試劑、Crypto Cel Antibody Reagent是UK DWI水質安全評估檢測的*抗體。

主要產品包括隱孢子蟲診斷試劑,賈第蟲診斷試劑,瘧疾診斷試劑,衣原體檢測試劑,絲蟲診斷試劑,錐蟲診斷試劑等。

廣州健侖生物科技有限公司與cellabs達成代理協議,歡迎廣大用戶咨詢訂購。

我司還提供其它進口或國產試劑盒:登革熱、瘧疾、流感、A鏈球菌、合胞病毒、腮病毒、乙腦、寨卡、黃熱病、基孔肯雅熱、克錐蟲病、違禁品濫用、肺炎球菌、軍團菌、化妝品檢測、食品安全檢測等試劑盒以及日本生研細菌分型診斷血清、德國SiFin診斷血清、丹麥SSI診斷血清等產品。

歡迎咨詢

歡迎咨詢2042552662

【Seracare產品介紹】

貨號

產品名稱

產品描述

規格

免疫熒光試劑盒(IFA kit)

KR1

Crypto Cel

隱孢子蟲(Cryptosporidium)間接免疫熒光檢測試劑

50 Test

KR2

Crypto/Giardia Cel

隱孢子蟲&賈第蟲(Cryptosporidium & Giardia)間接免疫熒光檢測試劑

50 Test

KG1

Giardia Cel

賈第蟲(Giardia)間接免疫熒光檢測試劑

50 Test

KC1

Chlamydia Cel

沙眼衣原體(Chlamydia trachomatis)間接免疫熒光檢測試劑

50 Test

KC2

Chlamydia Cel LPS

衣原體 lipopolysaccharide (LPS)間接免疫熒光檢測試劑

50 Test

KC3

Chlamydia Cel Pn

肺炎衣原體(Chlamydia pneumoniae)間接免疫熒光檢測試劑

50 Test

KP1

Pneumo Cel

卡氏肺孢子蟲(Pneumocystis carinii)間接免疫熒光檢測試劑

50 Test

KP2

Pneumo Cel Indirect

卡氏肺孢子蟲( Pneumocystis carinii)間接免疫熒光檢測試劑

50 Test

酶免試劑盒 ELISA kit

KG2

Giardia CELISA

賈第蟲(Giardia)ELISA kit

96 Test

KE1

Entamoeba CELISA Path

溶組織內阿米巴(Entamoeba histolytica) ELISA kit

96 Test

KF1 & KF2

Filariasis CELISA

班氏絲蟲(Wuchereria bancrofti ) ELISA kit

 

KM2

Malaria Antigen (HRP2) CELISA

惡性瘧原蟲(Plasmodium falciparum) 抗原 ELISA kit

192 Test

KMC3

Pan Malaria Antibody CELISA

間日、三日、惡性及卵形瘧疾(Malaria)ELISA IgG kit

192 Test

KT2

T. cruzi IgG CELISA

克氏錐蟲(Trypanosoma cruzi) ELISA IgG kit

192 Test

KT3

Toxocara IgG CELISA

弓首線蟲(Toxocara canis) ELISA IgG kit

192 Test

KF3

Filariasis Ab (Bm14) CELISA

淋巴絲蟲病(lymphatic filariasis) ELISA IgG kit

480 Test

KM7

Quantimal™ pLDH Malaria CELISA

瘧疾pLDH抗體檢測 ELISA kit

96 Test

 

二維碼掃一掃

【公司名稱】 廣州健侖生物科技有限公司
【】    楊永漢 
【】 
【騰訊 】 2042552662
【公司地址】 廣州清華科技園創新基地番禺石樓鎮創啟路63號二期2幢101-3室

【企業文化】

由此說明,紋狀體內存在乙酰膽堿遞質系統,其 功能的加強將導致震顫麻痹癥狀的出現。總結以上的研究結果,目前 認為黑質上行抵達紋狀體的多巴胺遞質系統的功能,在于抑制紋狀體 內乙酰膽堿遞質系統的功能;震顫麻痹患者由于多巴胺遞質系統功能 受損,導致乙酰膽堿遞質系統功能的亢進,才出現一系列癥狀。如果 應用左旋多巴以增強多巴胺的合成,或應用M型受體阻斷劑以阻斷乙酰 膽堿的作用,均能治療震顫麻痹。在正常情況下,黑質上行抵達紋狀 體的多巴胺遞質系統還與行為覺醒有關。動物實驗觀察到,單純破壞 中腦黑質多巴胺遞質系統后,則動物在行為上不能表現覺醒,對新異 的刺激不能表現探究行為。震顫麻痹患者面部表情呆板,可能就是行 為覺醒發生障礙的表現。舞蹈病患者的主要臨床表現為不自主的上肢 和頭部的舞蹈樣動作,并伴有肌張力降低等。病理研究證明,患者紋 狀體嚴重萎縮,而黑質-紋狀體通路是完好的。在這類患者,若采用左 旋多巴進行治療反而使癥狀加劇,而用利血平耗竭多巴胺遞質卻可使 癥狀緩解。神經生化的研究發現,患者紋狀體中膽堿能神經元和γ-氨 基丁酸能神經元的功能明顯減退。因此認為,舞蹈病病變主要是紋狀 體內的膽堿能和γ-氨基丁酸能神經元功能減退,而黑質多巴胺能神經 元功能相對亢進,這和震顫麻痹的病變機制正好相反。目前知道,黑 質和紋狀體之間是有環路的:黑質的多巴胺能上行系統能抑制紋 狀體內膽堿能和γ-氨基丁酸能系統的活動;而紋狀體的γ-氨基丁酸 下行系統能反饋抑制黑質的多巴胺能系統的活動(圖11-16)。臨床治 療震顫麻痹時,如左旋多巴用得過量則可引起類似舞蹈病的癥狀,也 說明上述的觀點是有道理的。殼核和尾狀核通過大量條紋狀細胞橋互 相連接,所以得名紋狀體。根據發生的早晚可分為新、舊紋狀體,新 紋狀體指豆狀核的殼和尾狀核,舊紋狀體指蒼白球,紋狀體屬錐體外 系的結構,與骨骼肌的活動有關。 在發生學上比較年輕,包括尾狀核 及殼核,它們起源于端腦。在這兩個神經細胞團中,含有大量的小細 胞和較少的大細胞。
This shows that there is an acetylcholine transmitter system in the striatum, and its enhanced function will lead to the appearance of paralysis symptoms. Summing up the above research results, it is currently believed that the function of the dopamine transmitter system of the substantia nigra arriving at the striatum is to inhibit the function of the acetylcholine transmitter system in the striatum; in patients with tremor paralysis, the function of the dopamine transmitter system is impaired, resulting in the transmission of acetylcholine. Only when the quality of the system functions, can a series of symptoms appear. If levodopa is used to enhance dopamine synthesis, or if an M-type receptor blocker is used to block the effects of acetylcholine, tremor paralysis can be treated. Under normal conditions, the dopamine transmitter system that the substantia nigra arrives at the striatum is also associated with behavioral arousal. Animal experiments have observed that after simply destroying the dopamine neurotransmitter system of the substantia nigra, the animals cannot behave awake in their behavior, and they can't express inquiry behavior for novel stimuli. The facial expression of a paralyzed paralyzed patient may be a manifestation of an arousal disorder. The main clinical manifestations of patients suffering from chorea are involuntary dance-like movements of the upper limbs and head, accompanied by decreased muscle tone. Pathological studies have demonstrated that the patient's striatum is severely atrophied and the nigro-striatal pathway is intact. In these patients, treatment with levodopa may worsen the symptoms, while depletion of dopamine transmitters with reserpine can relieve symptoms. Neurochemical studies have shown that the function of cholinergic and γ-aminobutyric acid neurons in the striatum of patients is significantly reduced. Therefore, it is believed that choriopathic lesions are mainly cholinergic and gamma-aminobutyric acid neuronal dysfunction in the striatum, and the substantia nigra dopaminergic neuronal function is relatively hyperactive, which is contrary to the pathogenesis of tremor paralysis. It is currently known that there is a looping link between the substantia nigra and the striatum: the dopaminergic ascending system of the substantia nigra inhibits the activity of cholinergic and gamma-aminobutyric acid energy systems in the striatum; whereas striatal The down-stream system of gamma-aminobutyric acid can feedback inhibit the activity of the dopaminergic system of the substantia nigra (Figure 11-16). When clinical therapy is used to paralyze paralysis, the use of excessive amounts of levodopa may cause symptoms similar to those of chorea. This also makes sense. The putamen and caudate nucleus are connected to each other by a large number of striped cell bridges, so the striatum is named. According to the occurrence of early and late can be divided into new and old striatum, the new striatum refers to the lenticular nucleus of the shell and caudate nucleus, the old striatum refers to the globus pallidus, striatum is the extrapyramidal structure, and skeletal muscle Related activities. It is relatively young in herogenesis, including caudate nucleus and putamen, which originated in the encephalon. In these two nerve cell clusters, there are a large number of small cells and fewer large cells.

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