Split Hand/foot Malformation (Ectrodactyly) Type 1 产品
(Split Hand/foot Malformation (Ectrodactyly) Type 1 (SHFM1))
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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. [provided by RefSeq, Jul 2008].
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Featured Split Hand/foot Malformation (Ectrodactyly) Type 1 Categories
Split Hand/foot Malformation (Ectrodactyly) Type 1 抗体
High quality antibodies with extensive validation data.
Split Hand/foot Malformation (Ectrodactyly) Type 1 ELISA试剂盒
Reliable ELISA kits for a wide range of species.
Split Hand/foot Malformation (Ectrodactyly) Type 1 蛋白
Proteins for various applications incl. WB, ELISA, IF etc.
Recommended Split Hand/foot Malformation (Ectrodactyly) Type 1 抗体
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Reactivity
Application
Validations
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Quantity
Datasheet
Reactivity
Human, Rat
Application
IHC, WB
Validations
- (2)
Cat. No.
ABIN6261375
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, IHC, WB, IF
Validations
Cat. No.
ABIN7119444
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Application
ELISA, ICC
Validations
Cat. No.
ABIN185118
Quantity
100 μg
Datasheet
Datasheet
Recommended Split Hand/foot Malformation (Ectrodactyly) Type 1 ELISA试剂盒
Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Analytical Method
Validations
Cat. No.
ABIN1118803
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Mouse
Analytical Method
Validations
Cat. No.
ABIN1118804
Quantity
96 tests
Datasheet
Datasheet
Reactivity
Cow
Analytical Method
Validations
Cat. No.
ABIN1118802
Quantity
96 tests
Datasheet
Datasheet
Recommended Split Hand/foot Malformation (Ectrodactyly) Type 1 蛋白
Latest Publications for our Split Hand/foot Malformation (Ectrodactyly) Type 1 Products
: "Identification of Dss1 as a 12-O-tetradecanoylphorbol-13-acetate-responsive gene expressed in keratinocyte progenitor cells, with possible involvement in early skin tumorigenesis." in: The Journal of biological chemistry, Vol. 278, Issue 3, pp. 1758-68, (2003) (PubMed).: "BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure." in: Science (New York, N.Y.), Vol. 297, Issue 5588, pp. 1837-48, (2002) (PubMed).
Synonyms and alternative names related to Split Hand/foot Malformation (Ectrodactyly) Type 1
SEM1, 26S proteasome complex subunit (SEM1), SEM1, 26S proteasome complex subunit (Sem1), SEM1, 26S proteasome complex subunit S homeolog (sem1.S), SEM1, 26S proteasome complex subunit (sem1), DSS1, Dss1, dss1, ECD, ecd, SEM1, sem1, SHFD1, shfd1, Shfdg1, shfdg1, Shfg, SHFM1, shfm1, shfm1.S, SHSF1, shsf1, wu:fb55c02, zgc:56203, zgc:85901Protein level used designations for Split Hand/foot Malformation (Ectrodactyly) Type 1
- 26S proteasome complex subunit DSS1
- deleted in split hand/split foot protein 1
- deleted in split-hand/split-foot 1
- split hand/foot deleted protein 1
- split hand/foot malformation type 1 protein
- candidate for split hand/foot malformation type 1
- 26 proteasome complex subunit DSS1
- split hand/foot malformation type 1 protein homolog
- split hand/foot malformation (ectrodactyly) type 1
- deleted in split hand/split foot protein 1 homolog
- split hand/foot deleted gene 1
- split hand/foot deleted protein 1 homolog
- 26S proteasome complex subunit SEM1
- split hand/foot malformation (ectrodactyly) type 1 S homeolog
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