CoraLite® Plus 488-conjugated SURF1 Recombinant antibody
SURF1 Recombinant Antibody for FC (Intra)
Host / Isotype
Rabbit / IgG
Reactivity
human
Applications
FC (Intra)
Conjugate
CoraLite® Plus 488 Fluorescent Dye
CloneNo.
230210E12
Cat no : CL488-83052-6
Synonyms
Validation Data Gallery
Tested Applications
Positive FC (Intra) detected in | HepG2 cells |
Recommended dilution
Application | Dilution |
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Flow Cytometry (FC) (INTRA) | FC (INTRA) : 0.80 ug per 10^6 cells in a 100 µl suspension |
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
Sample-dependent, Check data in validation data gallery. |
Product Information
CL488-83052-6 targets SURF1 in FC (Intra) applications and shows reactivity with human samples.
Tested Reactivity | human |
Host / Isotype | Rabbit / IgG |
Class | Recombinant |
Type | Antibody |
Immunogen | SURF1 fusion protein Ag3959 |
Full Name | surfeit 1 |
Calculated Molecular Weight | 33 kDa |
Observed Molecular Weight | 30-31 kDa |
GenBank Accession Number | BC028314 |
Gene Symbol | SURF1 |
Gene ID (NCBI) | 6834 |
Conjugate | CoraLite® Plus 488 Fluorescent Dye |
Excitation/Emission Maxima Wavelengths | 493 nm / 522 nm |
Form | Liquid |
Purification Method | Protein A purification |
Storage Buffer | PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3. |
Storage Conditions | Store at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. |
Background Information
SURF1 (Surfeit locus protein 1), also known as SURF-1. It is expected to be located in mitochondrion inner membrane, which is ubiquitinated in thyroid and kidney. This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency. The molecular weight of SURF1 is 33 kDa.
Protocols
Product Specific Protocols | |
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FC protocol for CL Plus 488 SURF1 antibody CL488-83052-6 | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |