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产地 | 上海 |
品牌 | OminimAbs |
保存条件 | |
货号 | OM641708 |
用途 | 实验研究 |
应用范围 | 科研实验 |
抗原来源 | 电询 |
保质期 | 2年 |
抗体名 | 电询 |
是否单克隆 | 否 |
克隆性 | 否 |
靶点 | 电询 |
适应物种 | 电询 |
形态 | 电询 |
宿主 | 电询 |
标记物 | 电询 |
包装规格 | 毫升 |
亚型 | 电询 |
标识物 | 电询 |
浓度 | 电询% |
免疫原 | 电询 |
是否进口 | 否 |
Product Profile
Product Name |
Anti-SHH antibody |
Antibody Type |
Primary Antibodies |
Immunogen |
Polypeptide |
Key Feature
Clonality |
Polyclonal |
Isotype |
IgG |
Host Species |
Rabbit |
Tested Application |
ELISAICC/IFWB |
WB:1:200-1:2000 |
|
Species Reactivity |
HumanMouseRat |
Concentration |
1 mg/ml |
Purification |
Protein A |
Target Information
Gene Symbol |
SHH |
Gene Synonyms |
TPT Hide |
Gene Full Name |
sonic hedgehog signaling molecule |
Gene Summary |
This gene encodes a protein that is instrumental in patterning the early embryo. It has been implicated as the key inductive signal in patterning of the ventral neural tube, the anterior-posterior limb axis, and the ventral somites. Of three human proteins showing sequence and functional similarity to the sonic hedgehog protein of Drosophila, this protein is the most similar. The protein is made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the developing embryo. Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE), a disorder in which the developing forebrain fails to correctly separate into right and left hemispheres. HPE is manifested by facial deformities. It is also thought that mutations in this gene or in its signalling pathway may be responsible for VACTERL syndrome, which is characterized by vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, radial and renal dysplasia, cardiac anomalies, and limb abnormalities. Additionally, mutations in a long range enhancer located approximately 1 megabase upstream of this gene disrupt limb patterning and can result in preaxial polydactyly. [provided by RefSeq, Jul 2008] Hide |
Molecular Weight(MW) |
50 kDa |
Cellular Localizatio |
Cell membrane, Membrane |
Application
·
WB
Western blot analysis using SHH antibody against A431(1) cell lysate.
·
ICC/IF
Immunofluorescence analysis of MG-63 cells using SHH antibody (green). Blue: DAPI fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor- 555 phalloidin.
Application Notes |
WB:1:200-1:2000 |
Additional Information
Form |
Liquid |
Storage Instruction |
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C long term. Avoid freeze / thaw cycle. |
Storage Buffer |
Purified antibody in PBS with 0.05% sodium azide. |
什么样的检验要求?要出示什么吗?
怎样算是处理过?还是就只是离心保存?
答:离心保存,检验要求,就是标本标号,和特殊要求
问:测好多指标 血清不分开可以么?
答:要分开,分好后,分别标上序列号,便于实验好区分。