癌症的基本特征包括细胞增殖、血管生成、迁移、凋亡逃避机制和细胞永生等。找到癌症发生过程中这些通路的关键标记物和对应的抗体用于检测至关重要。
为您推荐一个泛素化位点预测神器——泛素化分析工具，可以为您的蛋白的泛素化位点作出预测和评分。
细胞自噬受体图形绘图工具为你的蛋白的细胞受体结合位点作出预测和评分，识别结合到自噬通路中的蛋白是非常重要的，便于让我们理解自噬在正常生理、病理过程中的作用，如发育、细胞分化、神经退化性疾病、压力条件下、感染和癌症。
HCCS Antibody (Center) 精选
Affinity Purified Rabbit Polyclonal Antibody (Pab)
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- 背景知识
Application 
| IHC-P, WB, E |
|---|---|
| Primary Accession | P53701 |
| Other Accession | Q5F339, A5PJG7 |
| Reactivity | Human |
| Predicted | Bovine, Chicken, Mouse, Rat, Canine, Rabbit |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | Rabbit IgG |
| Calculated MW | 30602 Da |
| Antigen Region | 173-200 aa |
| Gene ID | 3052 |
|---|---|
| Other Names | Cytochrome c-type heme lyase, CCHL, Holocytochrome c-type synthase, HCCS, CCHL |
| Target/Specificity | This HCCS antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 173-200 amino acids from the Central region of human HCCS. |
| Dilution | IHC-P~~1:100~500 WB~~1:4000 E~~Use at an assay dependent concentration. |
| Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
| Precautions | HCCS Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
For Research Use Only. Not For Use In Diagnostic Procedures.
| Name | HCCS (HGNC:4837) |
|---|---|
| Synonyms | CCHL |
| Function | Lyase that catalyzes the covalent linking of the heme group to the cytochrome C apoprotein to produce the mature functional cytochrome. |
| Cellular Location | Mitochondrion inner membrane. Membrane; Lipid-anchor |
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene.
REFERENCES
Need, A.C., et al. Hum. Mol. Genet. 18(23):4650-4661(2009)
Wimplinger, I., et al. Mol. Vis. 13, 1475-1482 (2007)
Wimplinger, I., et al. Am. J. Hum. Genet. 79(5):878-889(2006)
Nakashima-Kamimura, N., et al. J. Cell. Sci. 118 (PT 22), 5357-5367 (2005)
Prakash, S.K., et al. Hum. Mol. Genet. 11(25):3237-3248(2002)
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