吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
又硬又粗又大一区二区三区视频 ,在线视频免费观看WWW动漫
Rabbit Anti-CYB5R3/PE-Cy5.5 Conjugated antibody (bs-12162R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-12162R-PE-Cy5.5
英文名稱1 Rabbit Anti-CYB5R3/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5標(biāo)記的細(xì)胞色素b5還原酶3抗體
別    名 B5R; Cyb5r3; Cytochrome b5 reductase 3; Cytochrome b5 reductase; DIA1; Diaphorase 1; Diaphorase-1; NADH cytochrome b5 reductase 3; NADH-cytochrome b5 reductase 3 membrane-bound form; NADH-cytochrome b5 reductase 3 soluble form; NB5R3_HUMAN; OTTHUMP00000028761; OTTHUMP00000198435; OTTHUMP00000198574; OTTHUMP00000198662; OTTHUMP00000198665.  
規(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 心血管  細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  脂蛋白  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Sheep, )
產(chǎn)品應(yīng)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 34kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CYB5R3
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 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.
產(chǎn)品介紹 background:
CYB5R3 is a 301 amino acid protein encoded by the human gene CYB5R3. CYB5R3 belongs to the flavoprotein pyridine nucleotide cytochrome reductase family and has two naturally occuring isoforms. Isoform 1 is anchored to the cytoplasmic side of the endoplasmic reticulum membrane and mitochondrion outer membrane, while isoform 2 is the soluble form found in erythrocytes. CYB5R3 is involved in the desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism and, in erythrocytes, methemoglobin reduction. A serine residue at position 117 seems to only be found in persons of African origin. The allele frequency is 0.23 in African Americans. It is not found in Caucasians, Asians, Indo-Aryans or Arabs. This difference seems to have no effect on the enzyme activity. Defects in CYB5R3 are the cause of hereditary methemoglobinemia (HM). There are three forms of this disease: type 1 (HM1), in which the enzyme is only deficient in erythrocytes with a mild cyanosis; type 2 (HM2), in which the enzyme is completely deficient; and type 3 (HM3), where the deficiency is seen in all blood cells. Type 2 is a severe form accompanied by mental retardation and neurological impairment.

Function:
Desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism, and, in erythrocyte, methemoglobin reduction.

Subunit:
Component of a complex composed of cytochrome b5, NADH-cytochrome b5 reductase (CYB5R3) and MOSC2 (By similarity).

Subcellular Location:
Endoplasmic reticulum membrane. Mitochondrion outer membrane and Cytoplasm. Produces the soluble form found in erythrocytes.

Tissue Specificity:
Isoform 2 is expressed at late stages of erythroid maturation.

DISEASE:
Defects in CYB5R3 are the cause of methemoglobinemia CYB5R3-related (METHB-CYB5R3) [MIM:250800]. A form of methemoglobinemia, a hematologic disease characterized by the presence of excessive amounts of methemoglobin in blood cells, resulting in decreased oxygen carrying capacity of the blood, cyanosis and hypoxia. There are two types of methemoglobinemia CYB5R3-related. In type 1, the defect affects the soluble form of the enzyme, is restricted to red blood cells, and causes well-tolerated methemoglobinemia. In type 2, the defect affects both the soluble and microsomal forms of the enzyme and is thus generalized, affecting red cells, leukocytes and all body tissues. Type 2 methemoglobinemia is associated with mental deficiency and other neurologic symptoms.

Similarity:
Belongs to the flavoprotein pyridine nucleotide cytochrome reductase family. Contains 1 FAD-binding FR-type domain.

Database links:

Entrez Gene: 1727 Human

Entrez Gene: 25035 Rat

Omim: 613213 Human

SwissProt: P00387 Human

SwissProt: P20070 Rat

Unigene: 561064 Human

Unigene: 35994 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.xucheq.com 北京博奧森生物技術(shù)有限公司
通過國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號(hào): 00124Q34771R2M/1100
通過國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
金瓶悔1一5扬思敏完整版| 久久久久亚洲精品中文字幕| 精品无码一区二区三区爱欲| 国产乱子伦一区二区三区| 女人扒开屁股桶爽30分钟| 国产精品成熟老女人 | 性久久久久久久| www亚洲精品少妇裸乳一区二区| 色偷偷88888欧美精品久久久 | 久久精品国产亚洲7777| 亚洲精品乱码久久久久久自慰 | 高清视频在线观看| 免费无码国产V片在线观看 | 亚洲国产成人精品无码区在线观看| 中文无码AV一区二区三区| 香肠派对比赛服| 精品久久久久久综合日本| 久久久久亚洲精品中文字幕| 办公室双腿打开揉弄高潮淑芬 | 无套内谢的新婚少妇国语播放| 人妻少妇精品中文字幕AV蜜桃| 人与禽性视频77777| 啊灬啊别停灬用力啊黑人| 国产精品久久久久久妇女| NBA直播在线观看免费| 免费国产裸体美女视频全黄| 人妻妺妺窝人体色WWW聚色窝| 久久精品国产精品亚洲精品| 少妇又紧又色又爽又刺激视频| 成全动漫视频在线观看免费高清| 熟妇少妇任你躁在线无码| 人妻激情偷乱视频一区二区三区| 国产AV麻豆MAG剧集 | 天天做天天摸天天爽天天爱 | 最近免费中文字幕中文高清百度 | 99久久久无码国产精品不卡 | 国产精品无码免费专区午夜| 和山田进行LV999的恋爱| 女性女同性AⅤ免费观女性恋| 日韩精品一区二区三区在线观看| 亚洲熟妇少妇任你躁在线观看无码|