PLOD1 (N-term) Rabbit Polyclonal Antibody
CAT#: AP53354PU-N
PLOD1 (N-term) rabbit polyclonal antibody, Aff - Purified
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CNY 6314.00
货期*
2周
规格
Specifications
| Product Data | |
| Applications | FC, IHC, WB |
| Recommend Dilution | ELISA: 1/1000. Western Blot: 1/100-1/500. Flow Cytometry: 1/10-1/50. Immunohistochemistry on Paraffin Sections: 1/10-1/50. |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | KLH conjugated synthetic peptide between 73-102 amino acids from the N-terminal region of human PLOD1 / PLOD |
| Specificity | This antibody recognizes Human PLOD1 / PLOD (N-term). |
| Isotype | Ig |
| Formulation | PBS containing 0.09% (W/V) Sodium Azide as preservative State: Aff - Purified State: Liquid purified Ig fraction |
| Concentration | lot specific |
| Purification | Protein A column, followed by peptide affinity purification |
| Conjugation | Unconjugated |
| Storage Condition | Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. |
| Gene Name | procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 |
| Database Link | |
| Background | Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity. |
| Synonyms | Lysyl hydroxylase 1, LLH |
| Note | Molecular Weight: 83550 Da |
| Reference Data | |
| Protein Families | Druggable Genome |
| Protein Pathways | Lysine degradation |
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