2017最新高清无码网站,av777在线观看网站

您好，歡迎來(lái)到拜力生物網(wǎng)站！請(qǐng)登錄注冊(cè)

我的訂單 | 聯(lián)系我們 | 在線客服QQ：3012681483 | 客服電話：400-968-7988 | 工作時(shí)間：08:30-17:30

主營(yíng)產(chǎn)品： ELISA試劑盒、抗體、補(bǔ)體血清、兔補(bǔ)體、干擾素、小鼠測(cè)溫儀、進(jìn)口試劑、Quidel代理、Swant代理、PBL Assay Science代理

網(wǎng)站首頁(yè) 產(chǎn)品中心代理品牌新聞資訊資源中心關(guān)于我們

所在位置：首頁(yè) > 產(chǎn)品中心 > Antibodies > Antibodies產(chǎn)品

訂購(gòu)信息

上海拜力生物科技公司

Tel:400-968-7988 021-33779008

Anti-CCHL (R104) Antibody

品牌：Antibodies

貨號(hào)：

規(guī)格：50μl

貨期：

應(yīng)用：

咨詢(xún)客服

立即購(gòu)買(mǎi) 加入購(gòu)物車(chē)

Anti-CCHL (R104) Antibody

商品詳情參考文獻(xiàn) 相關(guān)資料

Overview

Name:	Anti-CCHL (R104) Antibody See all CCHL primary antibodies
Description:	Rabbit polyclonal antibody to CCHL (R104)
Specificity:	CCHL (R104) pAb detects endogenous levels of CCHL protein.
Applications:	WB, IHC, IF
Reactivity:	Human, Mouse, Rat
Immunogen:	Synthetic peptide, corresponding to amino acids 80-120 of Human CCHL.
Host:	Rabbit
Clonality:	Polyclonal
Conjugate:	Unconjugated
Molecular Weight:	~ 31 kDa
Purity:	The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Product Form:	1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.

Target

Function:	Links covalently the heme group to the apoprotein of cytochrome c.
Involvement in Disease:	Linear skin defects with multiple congenital anomalies 1: A disorder characterized by dermal, ocular, neurological and cardiac abnormalities. LSDMCA1 main features are unilateral or bilateral microphthalmia, linear skin defects in affected females, and in utero lethality for males. Skin defects are limited to the face and neck, consisting of areas of aplastic skin that heal with age to form hyperpigmented areas. Additional features in female patients include agenesis of the corpus callosum, sclerocornea, chorioretinal abnormalities, infantile seizures, congenital heart defect, mental retardation, and diaphragmatic hernia. Microphthalmia is a disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities.
Sequence Similarities:	Belongs to the cytochrome c-type heme lyase family.
Cellular Location:	Mitochondrion inner membrane. Membrane.
Database Links:	Entrez Gene: 3052?Human Entrez Gene: 15159?Mouse Entrez Gene: 317444?Rat Omim: 300056?Human SwissProt: P53701?Human SwissProt: P53702?Mouse Unigene: 211571?Human Unigene: 284033?Mouse Unigene: 162316?Rat
Synonyms:	CCHL Antibody CCHL_HUMAN Antibody cytochrome c heme-lyase Antibody Cytochrome c-type heme lyase Antibody DKFZp779I1858 Antibody EC 4.4.1.17 Antibody HCCS Antibody Holocytochrome c synthase Antibody Holocytochrome c synthase (cytochrome c heme lyase) Antibody Holocytochrome c type synthase Antibody Holocytochrome c-type synthase Antibody MCOPS7 Antibody OTTHUMP00000022903 Antibody OTTHUMP00000022904 Antibody OTTHUMP00000022905 Antibody OTTMUSP00000021173 Antibody OTTMUSP00000021174 Antibody RGD1563855 Antibody RP23-37L2.1 Antibody
Information:	Target information shown above is from the UniProt Consortium.