Home > Product > Antibody > Rabbit Anti-BMP15 antibody
BMP 15; BMP-15; BMP15; BMP15_HUMAN; Bone morphogenetic protein 15; GDF 9B; GDF-9B; GDF9B; Growth/differentiation factor 9B; ODG2; POF4.
Cat:
SL6612R
Species Reactivity:
Human,(predicted: Mouse,Rat,Chicken,Pig,Cow,Horse,Rabbit,Sheep,)
Immunogen:
KLH conjugated synthetic peptide derived from human BMP15:321-392/392
Format:
Liquid
Storage instructions:
Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
WB=1:500-2000ELISA=1:5000-10000not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Product Overview:
Sample: A549(Human) Cell Lysate at 40 ugPrimary: Anti-BMP15 (SL6612R) at 1/300 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 14 kDObserved band size: 14 kD
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Unit:
Price: $
Product PDFs
Datasheet:


The BMP15 protein is a member of the bone morphogenetic protein family which is part of the transforming growth factor beta superfamily. The transforming growth factor beta superfamily includes large families of growth and differentiation factors. It is thought that BMP15 may be involved in oocyte maturation and follicular development as a homodimer, or by forming heterodimers with a related protein, Gdf9.

Function:
May be involved in follicular development. Oocyte-specific growth/differentiation factor that stimulates folliculogenesis and granulosa cell (GC) growth.

Subunit:
Homodimer. But, in contrast to other members of this family, cannot be disulfide-linked.

Subcellular Location:
Secreted.

DISEASE:
Defects in BMP15 are the cause of ovarian dysgenesis type 2 (ODG2) [MIM:300510]; also known as X-linked hypergonadotropic ovarian dysgenesis or hypergonadotropic ovarian failure due to ovarian dysgenesis. Ovarian dysgenesis leads to ovarian failure and accounts for about half of the cases of primary amenorrhea.
Defects in BMP15 are the cause of premature ovarian failure type 4 (POF4) [MIM:300510]. An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol.

Similarity:
Belongs to the TGF-beta family.

SWISS:
O95972

Gene ID:
9210

Database links:

Entrez Gene: 9210 Human

Entrez Gene: 12155 Mouse

Entrez Gene: 59302 Rat

Omim: 300247 Human

SwissProt: O95972 Human

SwissProt: Q9Z0L4 Mouse

Unigene: 532692 Human

Unigene: 42160 Mouse



Picture

Sample:
A549(Human) Cell Lysate at 40 ug
Primary: Anti-BMP15 (SL6612R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 14 kD
Observed band size: 14 kD
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