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Invitrogen™ SHFM1 Polyclonal Antibody
Goat Polyclonal Antibody
Supplier: Invitrogen™ PA5142078
This item is not returnable.
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Description
This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:32,000. Preliminary analysis showed no signal in Western Blot.
The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle.
Specifications
SHFM1 | |
Polyclonal | |
Unconjugated | |
SEM1 | |
26S proteasome complex subunit DSS1; 26S proteasome complex subunit SEM1; C7orf76; Deleted in split hand/split foot protein 1; deleted in split hand/split foot protein 1 homolog; deleted in split-hand/split-foot 1; Dss1; ECD; Putative protein SEM1, isoform 2; Sem1; SHFD1; Shfdg1; Shfg; Shfm1; SHSF1; split hand/foot deleted gene 1; split hand/foot deleted protein 1; Split hand/foot deleted protein 1 homolog; split hand/foot malformation (ectrodactyly) type 1; split hand/foot malformation type 1 protein; Split hand/foot malformation type 1 protein homolog | |
Goat | |
Ammonium sulfate precipitation | |
RUO | |
0, 7979 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
Immunocytochemistry | |
0.5 mg/mL | |
TBS with 0.5% BSA and 0.02% sodium azide; pH 7.3 | |
P60896, Q6ZVN7 | |
SEM1 | |
Peptide with sequence C-RAELEKHGYKMETS. | |
100 μg | |
Primary | |
Human | |
Antibody | |
IgG |
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