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- 详细信息
- 技术资料
- 克隆性:
多克隆
- 抗体名:
Anti-TRPM1 antibody
- 适应物种:
人/动物/植物
- 浓度:
0.3 mg/ml
- 保存条件:
-20°C
- 规格:
25 μl/100 μl/200 μl
Anti-TRPM1 antibody
Cat. No. JLC160372
Package 25 μl/100 μl/200 μl
Storage -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Product overview
Description Anti-TRPM1 rabbit polyclonal antibody
Applications ELISA, IHC
Immunogen Synthetic peptide of human TRPM1
Reactivity Human, Mouse, Rat
Content 0.3 mg/ml
Host species Rabbit
Ig class Immunogen-specific rabbit IgG
Purification Antigen affinity purification
Target information
Symbol TRPM1
Full name transient receptor potential cation channel, subfamily M, member 1
Synonyms MLSN1; CSNB1C; LTRPC1
Swissprot Q7Z4N2
Target Background
This gene encodes a member of the transient receptor potential melastatin subfamily of transient receptor potential ion channels. The encoded protein is a calcium permeable cation channel that is expressed in melanocytes and may play a role in melanin synthesis. Specific mutations in this gene are the cause autosomal recessive complete congenital stationary night blindness-1C. The expression of this protein is inversely correlated with melanoma aggressiveness and as such it is used as a prognostic marker for melanoma metastasis.
Cat. No. JLC160372
Package 25 μl/100 μl/200 μl
Storage -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Product overview
Description Anti-TRPM1 rabbit polyclonal antibody
Applications ELISA, IHC
Immunogen Synthetic peptide of human TRPM1
Reactivity Human, Mouse, Rat
Content 0.3 mg/ml
Host species Rabbit
Ig class Immunogen-specific rabbit IgG
Purification Antigen affinity purification
Target information
Symbol TRPM1
Full name transient receptor potential cation channel, subfamily M, member 1
Synonyms MLSN1; CSNB1C; LTRPC1
Swissprot Q7Z4N2
Target Background
This gene encodes a member of the transient receptor potential melastatin subfamily of transient receptor potential ion channels. The encoded protein is a calcium permeable cation channel that is expressed in melanocytes and may play a role in melanin synthesis. Specific mutations in this gene are the cause autosomal recessive complete congenital stationary night blindness-1C. The expression of this protein is inversely correlated with melanoma aggressiveness and as such it is used as a prognostic marker for melanoma metastasis.
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Anti-TRPM1 antibody
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