FITC标记的碳酸酐酶4抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的碳酸酐酶4抗体

FITC标记的碳酸酐酶4抗体

商家询价

产品名称: FITC标记的碳酸酐酶4抗体

英文名称: Anti-CAIV/Carbonic Anhydrase IV/FITC

产品编号: HZ-8722R-FITC

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

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 Rabbit Anti-CAIV/Carbonic Anhydrase IV/FITC Conjugated antibody

FITC标记的碳酸酐酶4抗体

 

英文名称 Anti-CAIV/Carbonic Anhydrase IV/FITC
中文名称 FITC标记的碳酸酐酶4抗体
别    名 CA IV; CA4; CAH4_HUMAN; CAIV; Car4; Carbonate dehydratase IV; Carbonic anhydrase 4; Carbonic dehydratase; Carbonic dehydratase IV; EC 4.2.1.1; Retinitis pigmentosa 17 (autosomal dominant); RP17.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 细胞生物  神经生物学  干细胞  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, 
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 35kDa
性    状 Lyophilized or Liquid
浓    度 2mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human CAIV/Carbonic Anhydrase IV
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍 background:
Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. This gene encodes a glycosylphosphatidyl-inositol-anchored membrane isozyme expressed on the luminal surfaces of pulmonary (and certain other) capillaries and proximal renal tubules. Its exact function is not known; however, it may have a role in inherited renal abnormalities of bicarbonate transport. [provided by RefSeq, Jul 2008]

Function:
Reversible hydration of carbon dioxide. May stimulate the sodium/bicarbonate transporter activity of SLC4A4 that acts in pH homeostasis. It is essential for acid overload removal from the retina and retina epithelium, and acid release in the choriocapillaris in the choroid.

Subunit:
Interacts with SLC4A4.

Subcellular Location:
Cell membrane; Lipid-anchor › GPI-anchor

Tissue Specificity:
Expressed in the endothelium of the choriocapillaris in eyes (at protein level). Not expressed in the retinal epithelium at detectable levels.

DISEASE:
The disease is caused by mutations affecting the gene represented in this entry. Defective acid overload removal from retina and retinal epithelium, due to mutant CA4, is responsible for photoreceptor degeneration, indicating that impaired pH homeostasis is the most likely cause underlying the RP17 phenotype.
Disease description:A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.

Similarity:
Belongs to the alpha-carbonic anhydrase family.

Database links:

Entrez Gene: 762 Human

Entrez Gene: 12351 Mouse

Omim: 114760 Human

SwissProt: P22748 Human

SwissProt: Q64444 Mouse

Unigene: 89485 Human

Unigene: 1641 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
   

碳酸酐酶(CA)是一类催化二氧化碳可逆水合的锌金属酶。它们参与多种生物过程,包括呼吸、钙化、酸碱平衡、骨吸收以及房水、脑脊液、唾液和胃酸的形成。它们表现出广泛的多样性在组织分布和亚细胞定位。该基因编码糖基磷脂酰肌醇锚定膜同工酶,表达于肺(和某些其它)毛细血管和近端肾小管的管腔表面。它的确切功能尚不清楚,但是,它可能在遗传性碳酸氢盐转运肾脏异常中起作用。[ RefSeq,JUL 2008 ]