产品: c-Kit 抗体
货号: AF6153
描述: Rabbit polyclonal antibody to c-Kit
应用: WB IHC IF/ICC
文献验证: WB, IF/ICC
反应: Human, Mouse, Rat
预测: Pig, Bovine, Horse, Rabbit, Dog
蛋白号: P10721
RRID: AB_2835024

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human, Mouse, Rat
克隆:
Polyclonal
特异性:
c-Kit Antibody detects endogenous levels of total c-Kit.
RRID:
AB_2835024
引用格式: Affinity Biosciences Cat# AF6153, RRID:AB_2835024.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

C Kit; c-Kit; c-Kit Ligand; CD117; Kit; Kit Ligand; KIT oncogene; KIT proto oncogene receptor tyrosine kinase; KIT_HUMAN; Mast cell growth factor receptor; Mast/stem cell growth factor receptor Kit; MGF; p145 c-kit; PBT; Piebald trait protein; Proto oncogene c Kit; Proto oncogene tyrosine protein kinase Kit; Proto-oncogene c-Kit; SCF Receptor; SCFR; soluble KIT variant 1; Steel Factor Receptor; Stem cell factor receptor; tyrosine protein kinase Kit; Tyrosine-protein kinase Kit; v kit Hardy Zuckerman 4 feline sarcoma viral oncogene homolog; v kit Hardy Zuckerman 4 feline sarcoma viral oncogene like protein; v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog;

抗原和靶标

免疫原:

A synthesized peptide derived from human c-Kit, corresponding to a region within the internal amino acids.

基因/基因ID:
描述:
KIT encodes the human homolog of the proto-oncogene c-kit. C-kit was first identified as the cellular homolog of the feline sarcoma viral oncogene v-kit. KIT is a type 3 transmembrane receptor for MGF (mast cell growth factor, also known as stem cell factor). Mutations in KIT are associated with gastrointestinal stromal tumors, mast cell disease, acute myelogenous lukemia, and piebaldism.

研究领域

· Environmental Information Processing > Signal transduction > MAPK signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > Ras signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > Rap1 signaling pathway.   (View pathway)

· Environmental Information Processing > Signaling molecules and interaction > Cytokine-cytokine receptor interaction.   (View pathway)

· Environmental Information Processing > Signal transduction > Phospholipase D signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > PI3K-Akt signaling pathway.   (View pathway)

· Human Diseases > Cancers: Overview > Pathways in cancer.   (View pathway)

· Human Diseases > Cancers: Specific types > Acute myeloid leukemia.   (View pathway)

· Human Diseases > Cancers: Specific types > Breast cancer.   (View pathway)

· Human Diseases > Cancers: Overview > Central carbon metabolism in cancer.   (View pathway)

· Organismal Systems > Immune system > Hematopoietic cell lineage.   (View pathway)

· Organismal Systems > Endocrine system > Melanogenesis.

文献引用

1). Microbiota-derived H2S induces c-kit+ cDC1 autophagic cell death and liver inflammation in metabolic dysfunction-associated steatohepatitis. Nature communications, 2025 (PubMed: 40044736) [IF=16.6]

2). Upregulation of BCL-2 by acridone derivative through gene promoter i-motif for alleviating liver damage of NAFLD/NASH. NUCLEIC ACIDS RESEARCH, 2020 (PubMed: 32710621) [IF=16.6]

Application: WB    Species: human    Sample: HepG2

Figure 3. Effect of A22 on gene transcription and translation in HepG2 cells. The mRNA levels of BCL-2 and BAX (A), as well as C-KIT, KRAS, C-MYC and VEGF (B) in HepG2 cells were analyzed by using qRT-PCR after incubation with increasing concentration of A22 for 12 h. (C) Effects of A22 on protein expressions of C-MYC, VEGF, C-KIT and BCL-2 in the presence or absence of increasing concentration of A22 for 24 h, which were quantitatively analyzed (D).

3). Identification and validation of immune and diagnostic biomarkers for interstitial cystitis/painful bladder syndrome by integrating bioinformatics and machine-learning. Frontiers in immunology, 2025 (PubMed: 39917301) [IF=5.7]

4). Effects of icariin as a feed additive on the reproductive function in bucks (Capra hircus). Frontiers in veterinary science, 2024 (PubMed: 39575435) [IF=3.2]

Application: IF/ICC    Species: goat    Sample:

Figure 5. Effect of ICA administration on male germ cell markers of dairy goats. (A) Confocal microscopy analyzes the distribution of PGP9.5, DDX4, and c-Kit in the testes. (a) Immunofluorescence analysis showed the expression of PGP9.5 and DDX4. (b) The fluorescence intensity was analyzed on the yellow lines by Fiji software. (c) Immunofluorescence analysis showed the distribution of PGP9.5 and c-Kit. (d) The fluorescence intensity was analyzed on the yellow lines by Fiji software. (B) qPCR and western blot analyze the expression of mRNA and proteins. (a) The mRNA levels of PGP9.5, DDX4, and c-Kit were examined by qPCR. (b) Western blot analysis was performed to measure the expression of target proteins. β-actin was utilized as a loading control. (c) The histogram represents the quantification of proteins levels. Each value represents the mean ± SEM, **p 

5). Organoid models derived from patients with malignant phyllodes tumor of the breast. Breast Cancer Research and Treatment, 2023 (PubMed: 37204665) [IF=3.0]

6). Arctiin alleviates functional constipation by enhancing intestinal motility in mice. Experimental and Therapeutic Medicine, 2023 (PubMed: 37090075) [IF=2.4]

7). Cytological and spectroscopic characteristics of c‐KIT N822K mutation in core binding factor acute myeloid leukemia cells. Journal of Biophotonics, 2020 (PubMed: 32390317) [IF=2.0]

Application: WB    Species: human    Sample: AML cells

Figure 6. |The effects of genetic abnormality-induced cytological and spectral alterations in AML cells. (a) Ratio of clone formation. (b) Relative contents of Raman bands screened by CRT algorithm. (c) Western blot analysis showed the c-KIT and p-c-KIT expression, GAPDH served as loading control, along with (d) ratio of phosphorylated c-KIT to total c-KIT. *P<0.05.

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