MID1IP1 polyclonal, anti-human, mouse, rat
€305.00
In stock
SKU
BS60526
Background:
Mig12, also known as MID1IP1 (Mid1-interacting protein 1), gastrulation-specific G12-like protein or STRAIT11499, is a 183 amino acid nuclear and cytoplasmic protein that belongs to the SPOT14 family. Mig12 is thought to play a role in the stabilization of microtubules through interaction with Midline-1. The gene encoding Mig12 maps to human chromosome Xp11.4. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Alternative Name:
Mid1-interacting protein 1, Gastrulation-specific G12-like protein, Mid1-interacting G12-like protein, Protein STRAIT11499, Spot 14-related protein, S14R, Spot 14-R
Application Dilution: WB: 1:500~1:1000
Specificity: MID1IP1 polyclonal antibody detects endogenous levels of MID1IP1 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human MID1IP1
MW: ~ 20 kDa
Swis Prot.: Q9NPA3
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
Mig12, also known as MID1IP1 (Mid1-interacting protein 1), gastrulation-specific G12-like protein or STRAIT11499, is a 183 amino acid nuclear and cytoplasmic protein that belongs to the SPOT14 family. Mig12 is thought to play a role in the stabilization of microtubules through interaction with Midline-1. The gene encoding Mig12 maps to human chromosome Xp11.4. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Alternative Name:
Mid1-interacting protein 1, Gastrulation-specific G12-like protein, Mid1-interacting G12-like protein, Protein STRAIT11499, Spot 14-related protein, S14R, Spot 14-R
Application Dilution: WB: 1:500~1:1000
Specificity: MID1IP1 polyclonal antibody detects endogenous levels of MID1IP1 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human MID1IP1
MW: ~ 20 kDa
Swis Prot.: Q9NPA3
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1 mg/ml in Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.2.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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