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Invitrogen™ SHFM1 Polyclonal Antibody

Goat Polyclonal Antibody

Supplier:  Invitrogen™ PA5142078

Catalog No. PIPA5142078


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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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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